Category: 61-82-5

Formula: C2H4N4. In 2021.0 J MOL STRUCT published article about ANABOLIC-STEROIDS; DECANOATE; HEALTH in [Iqbal, Urooj; Choudhary, M. Iqbal; Yousuf, Sammer] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Sindh, Pakistan in 2021.0, Cited 30.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Co-crystals are emerging as members of supramolecular family having particular practical and fundamental significance for chemists, crystallographers, pharmaceutical scientists, and theoreticians. The presented study is focused to synthesize anti-cancer co-crystals of commercially available nandrolone (1), a synthetic anabolic-androgenic steroidal drug. Co-crystallization is done using economical and green grinding and reflux methods to obtain nandrolone (Nan): salicylic acid (Sal) and nandrolone (Nan): 3-amino-1,2,4-triazole (Triz) co-crystals, in 2:1 and 1:1 stoichiometric ratios, respectively. The structural analysis and characterization were carried out using single-crystal X-ray diffraction, and vibrational spectroscopy. Nandrolone (1) crystallizes in monoclinic P2(1) space group, while the co-crystal-I (Nan:Sal) and co-crystal-II (Nan:Triz), co-crystallized in the orthorhombic P2(1)2(1)2(1) space group. The intermolecular hydrogen bonds O-H center dot center dot center dot O, C-H center dot center dot center dot O, N-H center dot center dot center dot O, O-H center dot center dot center dot N, and N-H center dot center dot center dot N between the active pharmaceutical ingredient (nandrolone) and co-formers (salicylic acid, and 3-amino-1,2,4-triazole) stabilize the structures of cocrystals. In vibrational spectroscopy of co-crystal-I (Nan:Sal), the blue shifts in stretching frequencies of hydroxyl group from 3417.9 cm(-1) to 3427.8 cm(-1) further supported the hydrogen bond interactions between API and co-former. Similarly, in co-crystal-II (Nan:Triz) the NH2 stretching frequency from 3331.4- 3413.4 cm(-1) to 3312.7 cm(-1), supported the interaction of NH2 with API via intermolecular interaction. Nandrolone (1) and both co-crystals were found to be non-cytotoxic against 3T3 normal fibroblast cell line. Nandrolone (IC50 = 1.0 0.1 mu M), co-crystal-I (Nan:Sal) (IC50 = 1.6 +/- 0.3 mu M) and-II (Nan:Triz) (IC50 = 1.8 +/- 0.1 mu M) showed anti-cancer potential against cervical cancer HeLa cell line. While doxorubicin (IC50 = 1.2 +/- 0.2 mu M) was used as standard tested compound. SYNOPSIS Two new non-cytotoxic co-crystals of synthetic anabolic-androgenic steroidal drug nandrolone (Nan) with pharmaceutically acceptable salicylic acid (Sal), and triazole (Triz) were synthesized and their structures were elucidated using single-crystal X-ray diffraction, and vibrational spectroscopy. Quantitative analysis of -OH and -NH2 intermolecular interactions between API and co-former by Hirshfeld surface analysis further supported the role of various functionalities towards the stability of co-crystals. Both co-crystals were found to be non-cytotoxic against 3T3 normal fibroblast cell line. Co-crystal-I (Nan:Sal) and co-crystal-II (Nan:Triz) were found to be selectively active against HeLa cancer cell line (IC50 = 1.6 +/- 0.3 mu M), (IC50 = 1.8 +/- 0.1 mu M). (c) 2020 Elsevier B.V. All rights reserved.

Formula: C2H4N4. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Name: 1H-1,2,4-Triazol-5-amine. In 2019.0 SYNTHESIS-STUTTGART published article about KETONES; TRIAZOLOPYRIMIDINES; DERIVATIVES; PYRAZOLES in [Andrade, Valquiria P.; Mittersteiner, Mateus; Bonacorso, Helio G.; Frizzo, Clarissa P.; Martins, Marcos A. P.; Zanatta, Nilo] Univ Fed Santa Maria, Nucleo Quim Heterociclos NUQUIMHE, BR-97105900 Santa Maria, RS, Brazil in 2019.0, Cited 30.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

The use of -enamino diketones as an easy entry to the regioselective synthesis of [1,2,4]triazolo[1,5- a ]pyrimidines is reported. These ketones reacted with 3-amino-1 H -1,2,4-triazoles to furnish exclusively 6-substituted 5-(trifluoromethyl)[1,2,4]triazolo[1,5- a ]pyrimidines in yields of up to 95%. The regioselectivity of the reactions performed was maintained regardless of the substituent in the starting ketone or aminoazole.

Name: 1H-1,2,4-Triazol-5-amine. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

In 2019.0 J MOL STRUCT published article about PHENOLIC SCHIFF-BASES; NMR CHEMICAL-SHIFTS; TRIAZOLOPYRIMIDINE; MECHANISM; APPROXIMATION; INHIBITORS; COMPLEXES; HERBICIDE; POTENT; SAR in [Lahmidi, Sanae; El Hafi, Mohamed; Boulhaoua, Mohammed; Essassi, El Mokhtar] Mohammed V Univ Rabat, Ctr Rech Sci Med, Pole Competences Pharmacochim, Lab Chim Organ Heterocycl,Fac Sci,URAC 21, Ave Ibn Battouta,BP 1014, Rabat, Morocco; [Anouar, El Hassane] Prince Sattam Bin Abdulaziz Univ, Coll Sci & Humanities, Dept Chem, BP 830, Al Kharj, Saudi Arabia; [Ejjoummany, Abdelaziz] Univ Hassan II Casablanca, EST Mohammedia, Lab Chim Phys & Chim Bioorgan, BP 146, Mohammadia 28800, Morocco; [El Jemli, Meryem] Mohammed V Univ, Fac Med & Pharm, Lab Pharmacol & Toxicol, Pharmacodynamy Res Team,ERP,Rabat Inst, BP 6203, Rabat, Morocco; [Mague, Joel T.] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA in 2019.0, Cited 60.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Two new (4-5) and a known (3) derivatives of 1,2,4-triazolo [1,5-a]pyrimidine are synthesized and characterized through spectroscopic NMR, FT-IR and single crystal X-ray diffraction techniques. Along with experimental data, the predicted spectral data are obtained using density functional theory (DFT) at the B3LYP/6-31 + G (d,p) level of theory. The closest contacts between active atoms of the compounds are identified through Hirshfeld surface analysis and electrostatic potential map (EPM) studies. Relatively, good correlations were found between the experimental and predicted spectroscopic data with correlation coefficients higher than 90%. Hirshfeld surface analysis and EPM reveal that the closest interaction between the units of the compounds are between hydrogen atoms (39.6-46.3%). The antioxidant activity of 3-5 is evaluated using DPPH free radical scavenging and ferric reducing antioxidant power assays. (C) 2018 Elsevier B.V. All rights reserved.

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Formula: C2H4N4. In 2020.0 WATER RES published article about DIFFERENT VALIDATION CRITERIA; REAL EXTERNAL PREDICTIVITY; CORRELATION-COEFFICIENT; IDENTIFICATION; ALTERNATIVES; EVALUATE; HAZARD in [Galimberti, Francesco; Moretto, Angelo] ASST Fatebenefratelli Sacco, Int Ctr Pesticides & Hlth Risk Prevent, ICPS, Milan, Italy; [Moretto, Angelo] Univ Milan, Dept Biomed & Clin Sci, Milan, Italy; [Papa, Ester] Univ Insubria, QSAR Res Unit Environm Chem & Ecotoxicol, Varese, Italy in 2020.0, Cited 45.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

The EFSA ‘Guidance on tiered risk assessment for edge-of-field surface waters’ underscores the importance of in silico models to support the pesticide risk assessment. The aim of this work was to use in silico models starting from an available, structured and harmonized pesticide dataset that was developed for different purposes, in order to stimulate the use of QSAR models for risk assessment. The present work focuses on the development of a set of in silico models, developed to predict the aquatic toxicity of heterogeneous pesticides with incomplete/unknown toxic behavior in the water compartment. The generated models have good fitting performances (R-2 : 0.75-0.99), they are internally robust (Q(2) loo: 0.66-0.98) and can handle up to 30% of perturbation of the training set (Q(2) Imo: 0.64-0.98). The absence of chance correlation was guaranteed by low values of R-2 calculated on scrambled responses (R-2 Y-scr: 0.11-0.38). Different statistical parameters were used to quantify the external predictivity of the models (CCCext: 0.73-0.91, Q(2) ext-Fn: 0.53-0.96). The results indicate that all the best models are predictive when applied to chemicals not involved in the models development. In addition, all models have similar accuracy both in fitting and in prediction and this represents a good degree of generalization. These models may be useful to support the risk assessment procedure when experimental data for key species are missing or to create prioritization lists for the general a priori assessment of the potential toxicity of existing and new pesticides which fall in the applicability domain. (C) 2020 Elsevier Ltd. All rights reserved.

Formula: C2H4N4. Welcome to talk about 61-82-5, If you have any questions, you can contact Galimberti, F; Moretto, A; Papa, E or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

An article Synthesis and application of amino triazolium-modified lactobionic acid as chiral selector in capillary electrophoresis WOS:000467665400021 published article about IONIC LIQUIDS; ENANTIOMERIC SEPARATION; BETA-CYCLODEXTRINS; ENANTIOSEPARATION; PERFORMANCE; COMPLEXES; MECHANISM; LIGAND; DRUGS; MODEL in [Liu, Jie; Du, Yingxiang; Sun, Xiaodong; Feng, Zijie; Ma, Xiaofei; Li, Jingtang] China Pharmaceut Univ, Dept Analyt Chem, 24 Tongjiaxiang, Nanjing 210009, Jiangsu, Peoples R China; [Du, Yingxiang] China Pharmaceut Univ, Minist Educ, Key Lab Drug Qual Control & Pharmacovigilance, Nanjing 210009, Jiangsu, Peoples R China; [Du, Yingxiang] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China in 2019.0, Cited 39.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

In this paper, a chiral selector, N-(4-H-1, 2, 4-triazolium)-lactobionamides (LA-ATM), was synthesized and applied for enantioseparation in capillary electrophoresis (CE) for the first time. Compared with lactobionic acid (LA) separation system, enhanced enantioseparation of five tested drugs was achieved in this modification system. In order to achieve good chiral separation, several parameters such as chiral selector concentration, buffer pH, applied voltage as well as the type and proportion of organic modifier were systematically investigated. Molecular modeling was applied to demonstrate the chiral recognition mechanism of the LA-ATM, which well supported the experimental results. Furthermore, a mathematical equation built up based on the molecular mechanics calculations was used in predicting resolution of tested drugs using LA or LA-ATM mediated CE, the predicted result was well correlated with the experimental result. (C) 2019 Published by Elsevier B.V.

Welcome to talk about 61-82-5, If you have any questions, you can contact Liu, J; Du, YX; Sun, XD; Feng, ZJ; Ma, XF; Li, JT or send Email.. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Recently I am researching about PLASMOPARA-VITICOLA; PESTICIDE-RESIDUES; CELLULOSE SYNTHASE; RESISTANCE; MECHANISMS; PATHOGEN; EXPOSURE; DEFENSE; DOMAIN; BIOSYNTHESIS, Saw an article supported by the Fondazione Cariplo (GraptaResistance)Fondazione Cariplo [Rif. 2015-0430]. Published in NATURE PORTFOLIO in BERLIN ,Authors: Colombo, M; Masiero, S; Rosa, S; Caporali, E; Toffolatti, SL; Mizzotti, C; Tadini, L; Rossi, F; Pellegrino, S; Musetti, R; Velasco, R; Perazzolli, M; Vezzulli, S; Pesaresi, P. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Recommanded Product: 1H-1,2,4-Triazol-5-amine

Grapevine (Vitis vinifera L.) is a crop of major economic importance. However, grapevine yield is guaranteed by the massive use of pesticides to counteract pathogen infections. Under temperate-humid climate conditions, downy mildew is a primary threat for viticulture. Downy mildew is caused by the biotrophic oomycete Plasmopara viticola Berl. & de Toni, which can attack grapevine green tissues. In lack of treatments and with favourable weather conditions, downy mildew can devastate up to 75% of grape cultivation in one season and weaken newly born shoots, causing serious economic losses. Nevertheless, the repeated and massive use of some fungicides can lead to environmental pollution, negative impact on non-targeted organisms, development of resistance, residual toxicity and can foster human health concerns. In this manuscript, we provide an innovative approach to obtain specific pathogen protection for plants. By using the yeast two-hybrid approach and the P. viticola cellulose synthase 2 (PvCesA2), as target enzyme, we screened a combinatorial 8 amino acid peptide library with the aim to identify interacting peptides, potentially able to inhibit PvCesa2. Here, we demonstrate that the NoPv1 peptide aptamer prevents P. viticola germ tube formation and grapevine leaf infection without affecting the growth of non-target organisms and without being toxic for human cells. Furthermore, NoPv1 is also able to counteract Phytophthora infestans growth, the causal agent of late blight in potato and tomato, possibly as a consequence of the high amino acid sequence similarity between P. viticola and P. infestans cellulose synthase enzymes.

Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.. Recommanded Product: 1H-1,2,4-Triazol-5-amine

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Recently I am researching about INDUCED LOCOMOTOR-ACTIVITY; ALDEHYDE DEHYDROGENASE; 3-NITROPROPIONIC ACID; REGIONAL-DISTRIBUTION; ALCOHOL-CONSUMPTION; CATALASE; ACETALDEHYDE; STRESS; OXIDATION; 3-AMINO-1,2,4-TRIAZOLE, Saw an article supported by the Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) from ArgentinaConsejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET); Secretaria de Ciencia y Tecnologia (SeCyT-UNC) from Argentina; Ministerio de Ciencia y Tecnologia de la Provincia de Cordoba (MinCyT) from Argentina; Fondo para la Investigacion Cientifica y Tecnologica (FONCyT) from Argentina. COA of Formula: C2H4N4. Published in ELSEVIER in AMSTERDAM ,Authors: Mattalloni, MS; Deza-Ponzio, R; Albrecht, PA; Fernandez-Hubeid, LE; Cancela, LM; Virgolini, MB. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Developmentally-lead (Pb)-exposed rats showed an enhanced vulnerability to the stimulating and motivational effects of ethanol (EtOH). This is accompanied by differential activity of the brain EtOH-metabolizing enzymes catalase (CAT) and mitochondrial aldehyde dehydrogenase (ALDH2). Based on the theory that brain acetaldehyde accumulation is associated with the reinforcing properties of EtOH, this study sought to determine brain CAT and ALDH2 expression in limbic areas of control and Pb-exposed animals after voluntary EtOH intake. Thirty-five-day-old rats perinatally exposed to 220 ppm Pb were offered with water or increasing EtOH solutions (2-10% v/v) during 28 days until postnatal day (PND) 63. Once intake was stable, the animals were administered: 1) saline (SAL; test days 21-24 or 21-28, as corresponds), or 2) a CAT inhibitor: 3-amine 1, 2, 4-triazole (AT; 250 mg/kg intraperitoneally [i.p.], 5 h before the last eight EtOH intake sessions -test days 21-24 and 25-28), or 3) a CAT booster: 3-nitropropionic acid (3NPA; 20 mg/kg subcutaneously [s.c.], 45 min before the last four EtOH intake sessions -test days 25-28). Two additional groups were centrally-administered cyanamide (CY, an ALDH2 inhibitor, 0.3 mg i.c.v. immediately before the last four EtOH sessions, test days 25-28) or its corresponding vehicle (VEH). Lead exposure increased EtOH intake, an effect potentiated in both groups by 3NPA or CY pretreatments and reduced by AT, albeit selectivity in the Pb group. Catalase abundance in limbic areas parallels these observations in the Pb group, showing higher CAT expression in all areas after EtOH consumption respect to the controls, an effect prevented by AT administration. In contrast, ALDH2 expression was reduced in the Pb animals after EtOH intake, with CY potentiating this effect in all brain areas under study. Based on these results and on previous evidences, we suggest that Pb exposure promotes acetaldehyde accumulation in limbic regions, providing some insights into the mechanism of action that underlies the vulnerability to the excessive EtOH consumption reported in these animals.

COA of Formula: C2H4N4. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

An article Screening and analysis of agouti signaling protein interaction partners in Pelodiscus sinensis suggests a role in lipid metabolism WOS:000541109300072 published article about DIABETES-MELLITUS; ADIPOSE-TISSUES; EXPRESSION; RECEPTOR; OBESITY; MOUSE; IDENTIFICATION; ASIP; VITRONECTIN; FILAMINS in [Zhang, Lili; Si, Yue-Xiu] Zhejiang Chinese Med Univ, Sch Basic Med Sci, Hangzhou 310053, Peoples R China; [Zhang, Lili; Yin, Shang-Jun; Zheng, Xiaoying; Chen, Xuanwei; Wang, Qian; Park, Yong-Doo; Qian, Guo-Ying] Zhejiang Wanli Univ, Coll Biol & Environm Sci, Ningbo 315100, Peoples R China; [Park, Yong-Doo] Tsinghua Univ, Skin Dis Res Ctr, Yangtze Delta Reg Inst, Jiaxing 314006, Peoples R China; [Park, Yong-Doo] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Dept Dermatol, Seoul 135710, South Korea in 2020.0, Cited 51.0. Recommanded Product: 61-82-5. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Agouti signaling protein (ASP) is a secreted paracrine protein that has been widely reported to function in melanogenesis and obesity and could potentially be a core protein that regulates the color and fatty phenotype of P. sinensis. In this study, we screened out interacting proteins of ASP by combined co-immunoprecipitation mass spectrometry (CoIP-MS), yeast two hybrid (Y2H) analysis, and computational predictions. We performed docking of ASP with its well-known receptor melanocortin receptor 4 (MC4R) to predict the binding capacity and to screen out actual ASP interacting proteins, CoIP-MS was performed where identified 32 proteins that could bind with ASP and Y2H confirmed seven proteins binding with ASP directly. CoIP-MS and Y2H screening results including PPI prediction revealed that vitronectin (VIN), apolipoprotein Al (AP0A1), apolipoprotein B (APOB), and filamin B (FLNB) were the key interacting proteins of ASP. VTN, AP0A1, and APOB are functional proteins in lipid metabolism and various skin disorders, suggesting ASP may function in lipid metabolism through these partners. This study provided protein-protein interaction information of ASP, and the results will promote further research into the diverse roles of ASP, as well as its binding partners, and their function in different strains of P. sinensis. (C) 2019 Published by Elsevier B.V.

Recommanded Product: 61-82-5. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

HPLC of Formula: C2H4N4. Nikoofar, K; Shahriyari, F in [Nikoofar, Kobra; Shahriyari, Fatemeh] Alzahra Univ, Fac Phys & Chem, Dept Chem, Tehran, Iran published Novel bio-based core-shell organic-inorganic nanohybrid from embedding aspartic acid-guanine ionic liquid on the hydroxylated nano silica surface (nano [(Asp-Gua) IL@PEG-SiO2]): A versatile nanostructure for the synthesis of bis(2,3-dihydroquinazolin-4(1H)-one) derivatives and tricarboxamides under green media in 2020.0, Cited 47.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

A new multi-layered nano structure has been prepared using hydroxylated nano silica (as core) and novel guaninium aspartate ionic liquid (as shell) (nano [(Asp-Gua) IL@PEG-SiO2]). It characterized by FT-IR, H-1 NMR, FESEM, EDAX, XRD, TGA/ DTG, and BET analysis. This bio-based organic-inorganic hybrid catalyzed synthesis of peptide-like tricarboxamides though the pseudo five-component condensation of aromatic aldehydes, aromatic amines, tert-butyl isocyanide, and Meldrum’s acid under green solventless conditions at room temperature successfully. Its efficacy affirmed in the preparation of bis (2,3-dihydroquinazolin-4(1H)-one) derivatives via one-pot pseudo five-component reaction of aldehydes, amines, and isatoic anhydride in 70 degrees C aqueous media. The protocol contains several advantages such as relatively short reaction times, simple work-up procedure, economic and environmentally-friend because of performing the two class of MCRs under green media, utilizing wide-range of substrates, and reusability and recoverability of the core-shell nano-promoter for 3 runs without significant activity loss. (C) 2020 Published by Elsevier Ltd.

HPLC of Formula: C2H4N4. Welcome to talk about 61-82-5, If you have any questions, you can contact Nikoofar, K; Shahriyari, F or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Recently I am researching about REDUCED GRAPHENE OXIDE; GOLD NANOPARTICLES; NANOCOMPOSITES; OXIDATION; BEHAVIOR; TETRAAMINOPHTHALOCYANINE; NANOSHEETS; REDUCTION; NANOTUBES; OXYGEN, Saw an article supported by the . Published in SPRINGER in NEW YORK ,Authors: Mafuwe, PT; Moyo, M; Mugadza, T; Shumba, M; Nyoni, S. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Cobalt oxide nanoparticles were anchored on polyaniline-appended cobalt phthalocyanine and used to modify glassy carbon electrodes for enhanced electrocatalytic oxidation of amitrole. The modified electrodes were characterised by cyclic voltammetry, electrochemical impedance spectroscopy and scanning electron microscopy. Cyclic voltammetry, linear sweep voltammetry, chronoamperometry and differential pulse voltammetry were used to evaluate the electrocatalytic behaviour of the designed sensors. Catalytic rate constant of 6.26×10(5)M(-1)s(-1) and apparent electron transfer rate constant of 8.84×10(-3)cms(-1) were observed on CoTCPc-PANI-Co3O4NP-GCE. The adsorption equilibrium constant and Gibbs energy were 4.8×10(1)M(-1) and -12.1kJmol(-1), respectively, confirming substrate adsorption during a spontaneous reaction on the surface of the modified electrode. The limit of detection and limit of quantification were 6.61×10(-8)M and 2×10(-7)M, respectively, for the electrocatalytic detection of amitrole and only suffered 4% signal loss after repetitive ten runs in 1mM amitrole.

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Mafuwe, PT; Moyo, M; Mugadza, T; Shumba, M; Nyoni, S or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics