Category: 61-82-5

I found the field of Biotechnology & Applied Microbiology; Plant Sciences very interesting. Saw the article A fungal effector and a rice NLR protein have antagonistic effects on a Bowman-Birk trypsin inhibitor published in 2020.0. Safety of 1H-1,2,4-Triazol-5-amine, Reprint Addresses Ning, YS (corresponding author), Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100193, Peoples R China.; Wang, GL (corresponding author), Ohio State Univ, Dept Plant Pathol, Columbus, OH 43210 USA.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Bowman-Birk trypsin inhibitors (BBIs) play important roles in animal and plant immunity, but how these protease inhibitors are involved in the immune system remains unclear. Here, we show that the rice (Oryza sativa) BBI protein APIP4 is a common target of a fungal effector and an NLR receptor for innate immunity. APIP4 exhibited trypsin inhibitor activityin vitroandin vivo. Knockout ofAPIP4in rice enhanced susceptibility, and overexpression ofAPIP4increased resistance to the fungal pathogenMagnaporthe oryzae. TheM. oryzaeeffector AvrPiz-t interacted with APIP4 and suppressed APIP4 trypsin inhibitor activity. By contrast, the rice NLR protein Piz-t interacted with APIP4, enhancing APIP4 transcript and protein levels, and protease inhibitor activity. Our findings reveal a novel host defence mechanism in which a host protease inhibitor targeted by a fungal pathogen is protected by an NLR receptor.

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhang, CY; Fang, H; Shi, XT; He, F; Wang, RY; Fan, JB; Bai, PF; Wang, JY; Park, CH; Bellizzi, M; Zhou, XP; Wang, GL; Ning, YS or concate me.

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

Product Details of 61-82-5. Authors Wang, GY; Zheng, T; Zhang, SQ; Ye, JW; Ning, GL in ELSEVIER published article about in [Ye, Junwei; Ning, Guiling] Dalian Univ Technol, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116012, Peoples R China; Dalian Univ Technol, Sch Chem Engn, 2 Linggong Rd, Dalian 116012, Peoples R China in 2021.0, 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 novel pyridinium salt derivative, 2,3,4,5,6-pentaphenyl-1-(1H-1,2,4-triazol-3-yl)pyridinium perchlorate (1) has been designed and synthesized by using pyrylium perchlorate and 3-amino-1H-1,2,4-triazole as ingredients, which can be exploited for the binding and specific sensing of anion via hydrogen bonds. Compound 1 exhibits intense blue emission in solution with maximum emission at 469 nm with a red shift relative to that (426 nm) of solid state. The luminescence intensity of 1 could be selectively and sensitivity quenched with acetate ion and fluorine ion among various anions including F-, Cl-, Br-, I-, AcO- and NO3-. Furthermore, the possible detection mechanism was investigated. This work could contribute a credible potential sensing application of 1,2,4-triazolyl substituted pentaphenylpyridinium salts towards the specific anions in biological and environmental concerns. (C) 2021 Elsevier B.V. All rights reserved.

Product Details of 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Wang, GY; Zheng, T; Zhang, SQ; Ye, JW; Ning, GL or concate me.

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. Nayak, A; Smetana, V; Mudring, AV; Rogers, RD in [Nayak, Amrita; Rogers, Robin D.] Univ Alabama, Coll Arts & Sci, Tuscaloosa, AL 35487 USA; [Smetana, Volodymyr; Mudring, Anja-Verena; Rogers, Robin D.] Stockholm Univ, Dept Mat & Environm Chem, S-10691 Stockholm, Sweden published Anhydrous vs Hydrated f-Element Acetate Polymers Dictated by the Stoichiometry of Protic Acidic/Basic Azole Mixtures in 2021.0, Cited 36.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Continuing our investigations of ionic liquid (IL) based routes to a library of f-element/soft donor complexes which could be studied crystallographically, we have explored the dissolution of f-element salts in protic imidazole-based ILs containing only soft donors at high temperatures to drive off volatiles, including water and carboxylic or mineral acids. Here we present our results, reacting acidic and basic azoles in 1:3 or 1:1 stoichiometric compositions at elevated temperature, followed by saturation with Nd(OAc)(3)center dot xH(2)O or Ce(OAc)(3)center dot xH(2)O, which led to 13 new metal-acetate polymeric complexes identified by single-crystal X-ray diffraction. We found that the diversity in coordination modes of the simple acetate ligand that interfere with substitution of the softer N donors led to several readily crystallizable complexes forming two distinct groups with respect to f-element interaction with the ionic liquid precursors. When the acidic/basic azole ratio was 1:3, acetate and a neutral basic azole were found to be coordinated to the metal centers but no water, although in one case (2) water was observed in the secondary coordination sphere: [Ce(mu(2)-OAc)(3)(C(1)im)](n) (1, C(1)im = 1-methylimidazole), [Nd(mu(2)-(OAc)(3)(C(1)im)](n)center dot nH(2)O (2), [Ce(mu(2)-OAc)(3)(C(2)im)](n) (3, C(2)im = 1-ethylimidazole), [Ln(mu(2)-OAc)(3)DMF](n) (Ln = Nd (4), Ce (5); dimethylformamide (DMF) was substituted for the azole mixture), and [Nd(mu(2)-OAc)(3)(C(4)im)](n) (6, C(4)im = 1-butylimidazole). However, when the stoichiometric ratio was 1:1, water was always observed coordinated to the metal ions with the acidic azole included in the structure as a solvate or cocrystal, despite a higher reaction temperature: [Nd(mu(2)-OAc)(3)(OH2)](n)center dot n(1,2,3-Taz) (7,1,2,3-Taz = 1,2,3-triazole), [Ln(mu(2)-OAc)(3)(OH2)](n)center dot n(4,5-DCim) (Ln = Nd (8), Ce (9), 4,5-DCim = 4,5-dicyanoimidazole), [Ln(mu(2)-OAc)(3)(OH2)](n)center dot n(3,5-diNH(2)-1,2,4-Taz) (Ln = Nd (10), Ce (11), 3,5diNH(2)-1,2,4-Taz = 3,5-diamino-1,2,4-triazole), [Ce(mu(2)-OAc)(3)(OH2)](n)center dot n(3-NH2-1,2,4-Taz) (12, 3-NH2-1,2,4-Taz = 3-amino-1,2,4-triazole), and [Nd(mu(2)-OAc)(3)(OH2)](n)center dot n(5-NH2-Tz) (13, 5-NH2-Tz = 5-aminotetrazole). All of the compounds retain the Ln:OAc- ratio of 1:3 and form 1D polymeric chains; however, they exhibit a variety of coordination modes affecting the degree of chain condensation. The isolation of both hydrated and anhydrous products revealed different abilities of the investigated soft N-donors to compete with O-donors finding their place in the coordination sphere of the lanthanide or in the crystal lattice.

Name: 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Nayak, A; Smetana, V; Mudring, AV; Rogers, RD or concate me.

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 Synergistic effect of Fe3O4 anchored N-doped rGO hybrid on mechanical, thermal and electromagnetic shielding properties of epoxy composites WOS:000467349000035 published article about REDUCED GRAPHENE; NANOCOMPOSITE; NANOPARTICLES; OXIDE in [Chhetri, Suman; Adak, Nitai Chandra; Samanta, Pranab; Murmu, Naresh Chandra; Kuila, Tapas] Council Sci & Ind Res Cent Mech Engn Res Inst, Surface Engn & Tribol Div, Durgapur 713209, India; [Chhetri, Suman; Adak, Nitai Chandra; Samanta, Pranab; Murmu, Naresh Chandra; Kuila, Tapas] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India; [Srivastava, Suneel Kumar] Indian Inst Technol Kharagpur, Dept Chem, Kharagpur 721302, W Bengal, India in 2019.0, Cited 42.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Computed Properties of C2H4N4

Herein, Fe3O4 nano-particles are anchored over nitrogen doped reduced graphene oxide Fe3O4@N-rGO) structure to accommodate electric and magnetic components, so that it could match both the conduction and polarization loss to augment the attenuation of electromagnetic radiation. The formation of condensed heteroaromatic structure and decoration of Fe3O4 particles on r-GO structure are confirmed by photoelectron spectroscopy (XPS). high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD). The Fe3O4@N-rGO hybrid is subsequently dispersed in epoxy matrix, which result in significantly higher electrical conductivity (1.31 s/m) and electromagnetic interference (EMI) shielding efficiency (- 26 dB at 1 mm thickness). It was assumed that presence of electric-magnetic integrated Fe3O4@N-rGO hybrid in epoxy matrix significantly improved the interfacial polarization and anisotropy energy, which was reflected in absorption loss value of -27 dB. The composites also exhibited enhanced mechanical and thermo-mechanical properties coupled with improved thermal stability.

Computed Properties of C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Chhetri, S; Adak, NC; Samanta, P; Murmu, NC; Srivastava, SK; Kuila, T or concate me.

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. Authors Ben Ali, A; El Bakri, Y; Lai, CH; Sebhaoui, J; El Ghayati, L; Essassi, E; Mague, JT in INT UNION CRYSTALLOGRAPHY published article about in [Ben Ali, Abdelkader] Mohammed V Univ Rabat, Fac Sci, Ctr Sci Mat, Lab Chim Appl Mat, Ave Ibn,BP 1014, Rabat, Morocco; [El Bakri, Youness; Sebhaoui, Jihad; El Ghayati, Lhoussaine; Essassi, El Mokhtar] Univ Mohammed 5, Fac Sci, Ctr Rech Sci Med, URAC 21,Pole Competence Pharmacochim, Av Ibn Battouta,BP 1014, Rabat, Morocco; [Lai, Chin-Hung] Chung Shan Med Univ, Dept Med Appl Chem, Taichung 40241, Taiwan; [Lai, Chin-Hung] Chung Shan Med Univ Hosp, Dept Med Educ, Taichung 40241, Taiwan; [Mague, Joel T.] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA in 2019.0, Cited 38.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In the title molecule, C13H16N4O3, the mean planes of the phenyl and triazole rings are nearly perpendicular to one another as a result of the intramolecular C-H center dot center dot center dot O and C-H center dot center dot center dot pi(ring) interactions. In the crystal, layers parallel to (101) are generated by O-H center dot center dot center dot N, N-H center dot center dot center dot O and N-H center dot center dot center dot N hydrogen bonds. The layers are connected by inversion-related pairs of C-H center dot center dot center dot O hydrogen bonds. The experimental molecular structure is close to the gas-phase geometryoptimized structure calculated by DFT methods. Hirshfeld surface analysis indicates that the most important interaction involving hydrogen in the title compound is the H center dot center dot center dot H contact. The contribution of the H center dot center dot center dot O, H center dot center dot center dot N, and H center dot center dot center dot H contacts are 13.6, 16.1, and 54.6%, respectively.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Ben Ali, A; El Bakri, Y; Lai, CH; Sebhaoui, J; El Ghayati, L; Essassi, E; Mague, JT or concate me.. HPLC of Formula: C2H4N4

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, Characterization, and DFT Calculations of Quinoline and Quinazoline Derivatives WOS:000579454600025 published article about DENSITY-FUNCTIONAL THERMOCHEMISTRY; BEARING BRIDGEHEAD NITROGEN; SPECTROSCOPIC CHARACTERIZATION; SMALL-MOLECULE; POTENT; OPTIMIZATION; INHIBITORS; AMETOCTRADIN; POLYMERASE; AGENTS in [Mohamed, H. S.] Beni Suef Univ, Res Inst Med & Aromat Plants, Bani Suwayf 62511, Egypt; [Abdel-Latif, M. K.; Ahmed, S. A.] Beni Suef Univ, Fac Sci, Dept Chem, Bani Suwayf 62511, Egypt in 2020.0, Cited 41.0. Quality Control of 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Treatment of 3-methylcyclohexanone with ethyl formate in the presence of sodium methoxide afforded sodium (2-methyl-6-oxocyclohexylidene)methanolate which reacted with aminopyrazoles, aminotriazole, and aminotetrazole to produce fused quinazoline derivatives; its reactions with cyanothioacetamide, cyanoacetamide, and cyanoacetohydrazide gave tetrahydroquinoline-3-carbonitrile derivatives. The reactions of 8-methyl-2-sulfanyl-5,6,7,8-tetrahydroquinoline-3-carbonitrile with alkylating agents led to the formation of thieno[2,3-b]quinoline derivatives. DFT computational studies of the synthesized compounds were carried out using B3LYP/6-311+G** and HF/6-311+G** approximations. The calculated HOMO and LUMO energies showed that charge transfer occurs in their molecules.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Mohamed, HS; Abdel-Latif, MK; Ahmed, SA or concate me.. Quality Control 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

An article Novel Pyruvate Kinase (PK) Inhibitors: New Target to Overcome Bacterial Resistance WOS:000520610800040 published article about TRANSITION-METAL COMPOUNDS; DENSITY-FUNCTIONAL THEORY; MOLECULAR-STRUCTURES; DOCKING; MOLYBDENUM; INDOLES; MANNICH; BONDS in [El Sayed, Mardia T.] Natl Res Ctr, Chem Ind Res Div, Appl Organ Chem Dept, Dokki 12311, Egypt; [Sarhan, Alaadin E.] Natl Res Ctr, Pharmaceut Div, Therapeut Chem Dept, Dokki 12311, Egypt; [Ahmed, Entsar] Al Azhar Univ, Chem Dept, Fac Sci, Girls Branch, Cairo, Egypt; [Khattab, Reham R.] Natl Res Ctr, Chem Ind Res Div, Photochem Dept, Dokki 12311, Egypt; [Elnaggar, Mohamed] Univ Sharjah, Fac Sci, Chem Dept, Sharjah 27272, U Arab Emirates; [El-Messery, Shahenda M.] Mansoura Univ, Fac Pharm, Dept Organ Pharmaceut Chem, POB 35516, Mansoura, Egypt; [Shaldam, Moataz A.] Kafrelsheikh Univ, Fac Pharm, Dept Pharmaceut Chem, Kafr Al Sheikh 33516, Egypt; [Hassan, Ghada S.] Mansoura Univ, Fac Pharm, Dept Med Chem, Mansoura 35516, Egypt in 2020.0, 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. Safety of 1H-1,2,4-Triazol-5-amine

In the present investigation, some novel nitro Mannich bases derived from Michael type addition of activated nitro olefin, beta-nitrostyrene with various amines either primary or secondary including some amino sugars were designed and synthesized. The produced Mannich bases have been full characterized through different spectroscopic techniques. Antimicrobial evaluation has been performed against the Gram positive S. aureus and methicillin-resistant S. aurues (MRSA) infections. 5 of the synthesized compounds represent the best candidates in the biological screening, they have exhibited good activity with MIC values range from 100 to 250 mu g/ml. The active agents have been tested for pyruvate kinase inhibition activity with % of inhibition range from 30 to 79 % with IC50 in a nano molar range. They also exhibited significant Pyruvate kinase inhibition in nanomolar range with IC50 of 1066, 662, 1887, 418 and 1128 ng/ml, respectively (versus 196 ng/ml for AZD7545). Molecular docking calculations for active agents were performed. A complete conformational analysis molecular modeling utilizing Gaussian 09 program (HF/DFT) was used to verify the mode of bonding through the optimized geometries as well as essential quantum parameters were calculated using frontier energies (EHOMO & ELUMO) for the active candidates indicating the overall stability of the structure.

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact El Sayed, MT; Sarhan, AE; Ahmed, E; Khattab, RR; Elnaggar, M; El-Messery, SM; Shaldam, MA; Hassan, GS or concate me.

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

Recommanded Product: 61-82-5. In 2019.0 J MOL STRUCT published article about METAL-COMPLEXES; ANTICANCER; TRIAZINES; CU(II); CO(II); SERIES; COPPER; MODEL; DNA in [Al-Khodir, Fatima A. I.; Al-Warhi, Tarfah; Abumelha, Hana M. A.; Al-Issa, S. A.] Princess Nourah Bint Abdulrahman Univ, Coll Sci, Dept Chem, Riyadh, Saudi Arabia in 2019.0, Cited 61.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

A series of vital complexes of [Se (L-n) (Cl)(x)]center dot yCl (where n = L-1, L-2, L-3 and L-4; x = 1, 2, or 3 and y = 1, 2, or 3) and [Ru (L-n) (Cl)(x) (H2O)(y)]zCl (where x = 2 or 3; y = 0,1 or 2 and z = 0 or 1) have been synthesized from the chemical reactions between ruthenium (III) or selenium (IV) salts and tri-substituted s-triazine derivatives (L-1 = N-2-(4-chlorophenyl)-N-4,N-6-di (pyrimidin-2-yl)-1,3,5-triazine-2,4,6-triamine; L-2 = N-2-(4-chlorophenyl)-N-4- (pyrimidin-2-yl)- N-6-(thiazol-2-yl)-1,3,5-triazine-2,4,6-triamine; L-3 = 6-chloro-N-2-(pyrimidin-2-yl)-N-4-(1H-1,2,4-triazol-3-yl)-1,3,5-triazine-2,4-diamine and L-4 = 6-chloro-N-2-(4-chlorophenyl)-N-4-(pyrimidin-2-yl)-1,3,5-triazine-2,4-diamine). The structural was investigated using of elemental analyses, molar conductance, IR, UV-Vis, magnetic susceptibility, H-1, C-13 NMR spectra and thermal analyses. The surface morphology behaviors of selenium (IV) and ruthenium (111) complexes were studied based on scanning and transmittance electron microscopes. The crystalline nature of s-triazine complexes have been investigated using X-ray powder diffraction spectra. Spectral results were concluded that the ligand acts as a neutral bidentate for (L-1 and L-4) and tridentate for (L-2 and L-3), and coordinates through the nitrogen atom of triazine ring and nitrogen atoms of (pyrimidine, thiazole, and triazole) rings towards metal ion. The cytotoxic IC50 results of the free L-n ligands and its selenium (IV) complexes in vitro against the human colon and lung cancer cell lines introduced a promising efficiency. (C) 2018 Elsevier B.V. All rights reserved.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Al-Khodir, FAI; Al-Warhi, T; Abumelha, HMA; Al-Issa, SA or concate me.. Recommanded Product: 61-82-5

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 DOSE-RESPONSE RELATIONSHIPS; DNA-DAMAGE; MOUSE LYMPHOMA; MUTAGENICITY; PERFORMANCE; GAMMA-H2AX; EXPRESSION; INDUCTION; DEPARTURE; TOXICITY, Saw an article supported by the . Quality Control of 1H-1,2,4-Triazol-5-amine. Published in SPRINGER HEIDELBERG in HEIDELBERG ,Authors: Seo, JE; Tryndyak, V; Wu, QG; Dreval, K; Pogribny, I; Bryant, M; Zhou, T; Robison, TW; Mei, N; Guo, XQ. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

In vitro genotoxicity testing that employs metabolically active human cells may be better suited for evaluating human in vivo genotoxicity than current bacterial or non-metabolically active mammalian cell systems. In the current study, 28 compounds, known to have different genotoxicity and carcinogenicity modes of action (MoAs), were evaluated over a wide range of concentrations for the ability to induce DNA damage in human HepG2 and HepaRG cells. DNA damage dose-responses in both cell lines were quantified using a combination of high-throughput high-content (HTHC) CometChip technology and benchmark dose (BMD) quantitative approaches. Assays of metabolic activity indicated that differentiated HepaRG cells had much higher levels of cytochromes P450 activity than did HepG2 cells. DNA damage was observed for four and two out of five indirect-acting genotoxic carcinogens in HepaRG and HepG2 cells, respectively. Four out of seven direct-acting carcinogens were positive in both cell lines, with two of the three negatives being genotoxic mainly through aneugenicity. The four chemicals positive in both cell lines generated HTHC Comet data in HepaRG and HepG2 cells with comparable BMD values. All the non-genotoxic compounds, including six non-genotoxic carcinogens, were negative in HepaRG cells; five genotoxic non-carcinogens also were negative. Our results indicate that the HTHC CometChip assay detects a greater proportion of genotoxic carcinogens requiring metabolic activation (i.e., indirect carcinogens) when conducted with HepaRG cells than with HepG2 cells. In addition, BMD genotoxicity potency estimate is useful for quantitatively evaluating CometChip assay data in a scientifically rigorous manner.

Quality Control of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Seo, JE; Tryndyak, V; Wu, QG; Dreval, K; Pogribny, I; Bryant, M; Zhou, T; Robison, TW; Mei, N; Guo, XQ or concate me.

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, structural investigation and NLO properties of three 1,2,4-triazole Schiff bases WOS:000569381800021 published article about POROUS COORDINATION POLYMER; CRYSTAL-STRUCTURE; SPECTROSCOPIC CHARACTERIZATION; MOLECULAR-STRUCTURE; ANTIOXIDANT ACTIVITY; BIOLOGICAL-ACTIVITY; COMPLEXES; PATTERNS; DOCKING; STORAGE in [Maza, Soumeya; Bouhidel, Zakaria; Cherouana, Aoutef] Univ Freres Mentouri Constantine 1, Dept Chim, Unite Rech Chim Environm & Mol Struct CHEMS, Constantine 25000, Algeria; [Maza, Soumeya; Pillet, Sebastien; Schaniel, Dominik; Guillot, Benoit; Bendeif, El-Eulmi] Univ Lorraine, CRM2, CNRS, Nancy, France; [Kijatkin, Christian; Imlau, Mirco] Osnabruck Univ, Sch Phys, D-49076 Osnabruck, Germany; [Kijatkin, Christian; Imlau, Mirco] Osnabruck Univ, Res Ctr Cellular Nanoanalyt, CellNanOs, D-49076 Osnabruck, Germany in 2020.0, 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

We report in this work the synthesis, crystal structures analyses, and nonlinear-optical (NLO) properties of three Schiff bases with halogens and triazole moieties: (E)-1-(4-bromophenyl)-N-(1H-1,2,4-triazol-3yl)methanimine L1, (E)-1-(4-bromophenyl)-N-(4H-1,2,4-triazol-3-yl)methanimine L2, and (E)-1-(4chlorophenyl)-N-(4H-1,2,4-triazol-3-yl)methanimine L3. The three molecules are built on the basis of the same backbone formed by two aromatic rings (phenyl and triazole) linked by imine bridge. The two first compounds L1 and L2 contain tautomers of the Schiff base, where a phenyl ring is substituted by a bromine atom. The third one, L3, is similar to L2 but contains a chlorine atom instead of bromine. In crystals formed by these three Schiff bases the three dimensional networks are formed by supramolecular interactions such as hydrogen bonds, C-X…pi and X…X (X = Cl or Br) contacts. Complementary Hirshfeld surface analyses were carried out to investigate and quantify the contributions of the different intermolecular interactions within the supramolecular assemblies. These analyses reveal that the main contributions in the studied compounds are provided by the H center dot center dot center dot H and N center dot center dot center dot H interactions that represent-53% (for L1),-49% (for L2) and-50% (for L3) of the total contributions to the Hirshfeld surface. The nonlinear optical properties are investigated by nonlinear diffuse femtosecond-pulse reflectometry and are compared with those of the reference material LiNbO3, in particular regarding the temporal evolution. (C) 2020 Elsevier B.V. All rights reserved.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Maza, S; Kijatkin, C; Bouhidel, Z; Pillet, S; Schaniel, D; Imlau, M; Guillot, B; Cherouana, A; Bendeif, EE or concate me.. 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