Tag: M.W=0-100

Recently I am researching about RESONANCE ENERGY-TRANSFER; GOLD NANOCLUSTERS; FLUORESCENT SENSOR; RESIDUE; NANOCRYSTALS; PESTICIDES; CELLS; SERUM; PROBE; WATER, Saw an article supported by the Shandong Provincial Natural Science FoundationNatural Science Foundation of Shandong Province [ZR2019MEM046]; Weifang University of Science and Technology Talent Project [2018RC004]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Liu, HJ; Dong, LB; Wang, M; Huang, GF. 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

Herein, a novel and sensitive fluorescence method for cartap determination is established on the basis of the inner filter effect (IFE) of gold nanoparticles (Au NPs) on the fluorescence of glutathione protected Cu NCs (GSH-Cu NCs). In the presence of Au NPs, the fluorescence of GSH-Cu NCs was strongly quenched by the IFE because the absorption spectra of Au NPs overlap well with the emission spectra of GSH-Cu NCs. Upon addition of cartap, cartap could induce the aggregation of Au NPs whose absorption spectrum does not overlap with the emission spectrum of GSH-Cu NCs. Then, with the increase in cartap concentration, the IFE-decreased fluorescence was gradually recovered, realizing the fluorescence sensing of cartap. Under optimal conditions, the proposed method has a good linear relationship with cartap concentration in the range of 7-100 nM, and the detection limit is 3.34 nM. In addition, satisfactory results were obtained for cartap analysis using tap water and cabbage as real samples, which demonstrated that the method as-developed would have great practical application prospects.

Welcome to talk about 61-82-5, If you have any questions, you can contact Liu, HJ; Dong, LB; Wang, M; Huang, GF 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 HETEROJUNCTION PHOTOCATALYSTS; COMPOSITE; WATER; DEGRADATION; NANOTUBES; EVOLUTION; SEMICONDUCTORS; OXIDATION; REDUCTION; PHENOL, Saw an article supported by the ARC Discovery ProjectsAustralian Research Council [DP14010243, DP190103720]; Macquarie University iMQRTP scholarship. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Kheradmand, A; Zhu, YX; Zhang, WW; Marianov, A; Jiang, YJ. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Computed Properties of C2H4N4

Cobalt oxide (Co3O4) nanoparticles decorated on mesoporous carbon nitride (Co3O4/MCN) nanocomposites for photocatalytic hydrogen evolution were investigated in this work. MCN was prepared using 3-amino-1,2,4-triazole, high nitrogen content, as a single molecular carbon and nitrogen precursor and SiO2 nanoparticles as the hard template. Complementary characterization techniques were employed to understand the textural and chemical properties of the nanocomposites. The bare MCN showed high photocatalytic activity under visible light irradiation without using any co-catalyst. The photocatalytic activity of Co3O4/MCN with a Co3O4 mass content of 5 wt % presented two times higher than the bare MCN, which is attributed to the enhanced visible-light harvesting and more efficient charge separation. Mechanistic study shows lower electron-hole recombination rate, higher charge separation efficiency occurs after the formation of p-n type heterojunction. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

Welcome to talk about 61-82-5, If you have any questions, you can contact Kheradmand, A; Zhu, YX; Zhang, WW; Marianov, A; Jiang, YJ or send Email.. Computed Properties of 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

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 in NATURE PORTFOLIO published article about PLASMOPARA-VITICOLA; PESTICIDE-RESIDUES; CELLULOSE SYNTHASE; RESISTANCE; MECHANISMS; PATHOGEN; EXPOSURE; DEFENSE; DOMAIN; BIOSYNTHESIS in [Colombo, Monica; Perazzolli, Michele; Vezzulli, Silvia] Fdn Edmund Mach, Res & Innovat Ctr, San Michele All Adige, Italy; [Masiero, Simona; Rosa, Stefano; Caporali, Elisabetta; Mizzotti, Chiara; Tadini, Luca; Pesaresi, Paolo] Univ Milan, Dept Biosci, Milan, Italy; [Toffolatti, Silvia Laura] Univ Milan, Dept Agr & Environm Sci DISAA, Milan, Italy; [Rossi, Fabio] Univ Milan, Ctr Study & Res Obes, Dept Med Biotechnol & Translat Med, Milan, Italy; [Pellegrino, Sara] Univ Milan, DISFARM Dept Pharmaceut Sci, Milan, Italy; [Musetti, Rita] Univ Udine, Dept Agr Food Environm & Anim Sci, Udine, Italy; [Velasco, Riccardo] CREA Res Ctr Viticulture & Enol, Conegliano, TV, Italy; [Perazzolli, Michele] Univ Trento, Ctr Agr Food Environm C3A, San Michele All Adige, Italy in 2020.0, Cited 81.0. SDS of cas: 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

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.

Welcome to talk about 61-82-5, If you have any questions, you can contact 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 or send Email.. SDS of cas: 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

HPLC of Formula: C2H4N4. In 2019.0 ENVIRON MICROBIOL published article about INTERSPECIES ELECTRON-TRANSFER; IV PILI; PROTEIN; REDUCTION; NANOWIRES; EXCHANGE; FE(III) in [Liu, Xing; Zhan, Ji; Jing, Xianyue; Zhou, Shungui] Fujian Agr & Forestry Univ, Coll Resources & Environm, Fujian Prov Key Lab Soil Environm Hlth & Regulat, Fuzhou, Fujian, Peoples R China; [Lovley, Derek R.] Univ Massachusetts, Dept Microbiol, Amherst, MA 01003 USA in 2019.0, Cited 44.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Mechanisms controlling the expression of the electrically conductive pili (e-pili) of Geobacter species are of interest because of the important role of e-pili in diverse biogeochemical processes, anaerobic digestion and electromicrobiological applications. We investigated the function of the protein, designated Spc (short pilin chaperone), encoded by the gene immediately downstream from the gene for PilA, the monomer that assembles into e-pili. Multiple lines of evidence suggest that Spc forms an oligomer that is associated with the inner membrane. Mutating the start codon of spc to prevent translation increased the transcript abundance of pilA but greatly diminished the abundance of PilA, and e-pili could no longer be detected. Cross-linking, protein capture and two-hybrid studies demonstrated that Spc and PilA interacted. Two sites in PilA for electrostatic interaction with Spc were identified. The results demonstrate that Spc is required for PilA stability prior to incorporation into e-pili, suggesting that Spc has a chaperone function that may be specific to the relatively short PilA monomers that assemble into e-pili. These results are important for identifying microorganisms likely to express e-pili from (meta)genomic data and for the construction of microbial strains expressing e-pili.

HPLC of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Liu, X; Zhan, J; Jing, XY; Zhou, SG; Lovley, DR 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. Recently I am researching about DENSITY-FUNCTIONAL THERMOCHEMISTRY; BEARING BRIDGEHEAD NITROGEN; SPECTROSCOPIC CHARACTERIZATION; SMALL-MOLECULE; POTENT; OPTIMIZATION; INHIBITORS; AMETOCTRADIN; POLYMERASE; AGENTS, Saw an article supported by the . Published in MAIK NAUKA/INTERPERIODICA/SPRINGER in NEW YORK ,Authors: Mohamed, HS; Abdel-Latif, MK; Ahmed, SA. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

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.. Product Details of 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

COA of Formula: C2H4N4. Authors Xu, XQ; Wu, P; Li, CY; Zhao, KY; Wang, CR; Deng, RP; Zhang, JL in AMER CHEMICAL SOC published article about in [Xu, Xiaoqing; Zhao, Keyong; Wang, Chiran; Deng, Renpan; Zhang, Jinli] Shihezi Univ, Key Lab Green Proc Chem Engn Xinjiang Bingtuan, Sch Chem & Chem Engn, Shihezi 832003, Peoples R China; [Wu, Peng] Soochow Univ, Sch Chem & Environm Engn, Suzhou 215123, Jiangsu, Peoples R China; [Li, Changyong] Univ Bremen, Ctr Appl Space Technol & Micrograv ZARM, D-28359 Bremen, Germany in 2021.0, Cited 59.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In this work, amine-functionalized ZIF8 (i.e., ZIF8-A) was dispersed in n-heptanol (ZIF8-A/n-heptanol) to remove SO2. The effects of ZIF8-A proportion, SO2 concentration, and absorption and desorption temperatures on the removal of SO2 were systematically investigated. The experimental results showed that the activity of ZIF8-A on SO2 removal was enhanced after being dispersed in n-heptanol. The SO2 saturation capacity increased with increasing proportion of ZIF8-A and SO(2)concentration. The optimal temperatures for SO2 absorption and desorption were found to be 25 and 120 degrees C, respectively. Under the optimal experimental conditions (25 degrees C and 4% SO2), the SO2 saturation capacity was 589 mg/g. Five continuous absorption-desorption cycles suggested a good regeneration performance. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, ultraviolet analyses, and computational simulation indicated that SO2 mainly interacted with ZIF8-A via hydrogen bonds besides physical absorption. The simulation results further indicated that the enhanced SO2 adsorption performance of ZIF8-A when dispersed in n-heptanol was due to the lower self-diffusion coefficient and higher isosteric heat of SO2 molecules in ZIF8-A/nheptanol.

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.. COA 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 Design, synthesis and biological evaluation of novel acetamide-substituted doravirine and its prodrugs as potent HIV-1 NNRTIs WOS:000455855200001 published article about REVERSE-TRANSCRIPTASE INHIBITOR; COLORIMETRIC ASSAY; PATENT EVALUATION; DISCOVERY; STRATEGIES; GW678248 in [Wang, Zhao; Yu, Zhao; Kang, Dongwei; Zhang, Jian; Tian, Ye; Zhan, Peng; Liu, Xinyong] Shandong Univ, Sch Pharmaceut Sci, Minist Educ, Dept Med Chem,Key Lab Chem Biol, 44 West Culture Rd, Jinan 250012, Shandong, Peoples R China; [Daelemans, Dirk; De Clercq, Erik; Pannecouque, Christophe] Katholieke Univ Leuven, Lab Virol & Chemotherapy, Rega Inst Med Res, Herestr 49 Postbus 1043 09-A097, B-3000 Leuven, Belgium in 2019.0, Cited 30.0. COA of Formula: C2H4N4. 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 series of acetamide-substituted derivatives and two prodrugs of doravirine were designed and synthesized as potent HIV-1 NNRTIs by employing the structure-based drug design strategy. In MT-4 cell-based assays using the MTT method, it was found that most of the new compounds exhibited moderate to excellent inhibitory potency against the wild-type (WT) HIV-1 strain with a minimum EC50 value of 54.8 nM. Among them, the two most potent compounds 8i (EC50 = 59.5 nM) and 8k (EC50 = 54.8 nM) displayed robust activity against WT HIV-1 with double-digit nanomolar EC50 values, being superior to lamivudine (3TC, EC50= 12.8 mu M) and comparable to doravirine (EC50= 13 nM). Besides, 8i and 8k shown moderate activity against the double RT mutant (K103N + Y181C) HIV-1 RES056 strain. The HIV-1 RT inhibition assay further validated the binding target. Molecular simulation of the representative compounds was employed to provide insight on their structure-activity relationships (SARs) and direct future design efforts. Finally, the aqueous solubility and chemical stability of the prodrugs 9 and 10 were investigated in detail.

COA of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Wang, Z; Yu, Z; Kang, DW; Zhang, J; Tian, Y; Daelemans, D; De Clercq, E; Pannecouque, C; Zhan, P; Liu, XY 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 Suzuki, S; Hasegawa, A; Uebori, M; Shinomiya, M; Yoshida, Y; Ookubo, K; Takino, M; Hasegawa, H; Takazawa, M; Takemine, S in WILEY published article about in [Suzuki, Shigeru; Uebori, Michiko; Takazawa, Mari] Chubu Univ, Grad Sch Biosci & Biotechnol, 1200 Matsumoto, Kasugai, Aichi 4878501, Japan; [Hasegawa, Atsuko] Kanagawa Environm Res Ctr, Environm Conservat Div, 1-3-39,Shinomiya, Hiratsuka, Kanagawa 2540014, Japan; [Shinomiya, Miho] Saitama Prefectural Univ, Sch Hlth & Social Serv, 820 Sannomiya, Koshigaya 3438540, Japan; [Yoshida, Yasuko] Sumica Chem Anal Serv Ltd, Environm Hlth & Safety Div, Bunkyo Ku, Sumitomo Fudosan Hongo Bldg 9F,22-5,Hongo 3 Chome, Tokyo 1130033, Japan; [Ookubo, Kaori] Saga Prefectural Inst Publ Hlth & Pharmaceut Res, Phys & Chem Res & Investigate Div, 1-20 Hacchonawatemachi, Saga 8490925, Japan; [Takino, Masahiko] Agilent Technol Japan Ltd, Chromatog & Mass Spectrometry Div, 9-1 Takakura Machi, Hachioji, Tokyo 1920033, Japan; [Hasegawa, Hitomi] Nagoya City Environm Sci Res Inst, Water Qual Div, Minami Ku, 5-16-8 Toyoda, Nagoya, Aichi 4570841, Japan; [Takazawa, Mari] Publ Works Res Inst, Water Environm Res Grp, 1-6 Minamihara, Tsukuba, Ibaraki, Japan; [Takemine, Shusuke] Ctr Environm Sci Saitama, Chem Subst Team, 914 Oaza Kamitanadare,Kisai Machi, Kazo, Saitama 3470115, Japan in 2021.0, Cited 41.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Despite the increasing detection of emerging substances in the environment, the identity of most are left unknown due to the lack of efficient identification methods. We developed a non-target analysis method for identifying unknown substances in the environment by liquid chromatography/high-resolution mass spectrometry (LC/HRMS) with a product ion and neutral loss database (PNDB). The present analysis describes an elucidation method with elemental compositions of the molecules, product ions, and corresponding neutral losses of the unknown substance: (1) with the molecular formula, possible molecular structures are retrieved from two chemical structure databases (PubChem and ChemSpider); then (2) with the elemental compositions of product ions and neutral losses, possible partial structures are retrieved from the PNDB; and finally, (3) molecular structures that match the possible partial structures are listed in order of number of hits. A molecular structure with a higher number of hits is more similar to the structure of the analyzed substance. The performance of the non-target method was evaluated by simulated analysis of 150 LC/HRMS spectra registered in MassBank. First, all substances of the same mass data (41/41) and 68% (39/57) of the mass data of the same substances not registered in the PNDB were elucidated. It was demonstrated that 14% (7/52) and 31% (16/52) of the substances with no mass spectral data registered in the PNDB were obtained at the first and within the fifth place, respectively. Owing to the fact that 10 of the total hits occurred in product ions and neutral losses, almost 50% of the substances evaluated with this method were placed at the top 4 positions in the similarity ranking. Importantly, the proposed method is effective for analyzing mass spectral data that has not been registered in the PNDB and thus is expected to be used for a variety of non-target analyses.

Product Details of 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Suzuki, S; Hasegawa, A; Uebori, M; Shinomiya, M; Yoshida, Y; Ookubo, K; Takino, M; Hasegawa, H; Takazawa, M; Takemine, S 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

I found the field of Microbiology very interesting. Saw the article Magnaporthe oryzae MoNdt80 is a transcriptional regulator of GlcNAc catabolic pathway involved in pathogenesis published in 2020.0. Safety of 1H-1,2,4-Triazol-5-amine, Reprint Addresses Narula, A (corresponding author), Jamia Hamdard, Dept Biotechnol, Sch Chem & Life Sci, New Delhi 110062, India.; Datta, A (corresponding author), Natl Inst Plant Genome Res, Aruna Asaf Ali Marg, New Delhi 110067, India.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Availability and efficient utilization of host-derived nutrients by pathogens decide the fate of host-pathogen interaction. In Magnaporthe oryzae, N-acetylglucosamine (GlcNAc) catabolic pathway was found essential for successful host colonization and pathogenicity. GlcNAc catabolic enzymes hexokinase, GlcNAc-6-phosphate deacetylase (MoDac) and GlcN-6-phosphate deaminase (MoDeam) are encoded in a genomic cluster in M. oryzae and several phytopathogenic fungi. However, transcriptional regulation of GlcNAc catabolic pathway was not understood. We identified a conserved Ndt80/PhoG-like transcriptional regulator as a part of the GlcNAc catabolic gene cluster in M. oryzae and other fungi. We found that MoNdt80 is essential for GlcNAc utilization and pathogenicity of M. oryzae. Unlike WT, Delta MoNdt80 failed to induce transcription of GlcNAc catabolic pathway genes in response to GlcNAc. MoNdt80 could bind to a specific cis-acting consensus sequence GNCRCAAA[AT], present in the promoter of MoDac, MoDeam and beta-hexosaminidase (MoHex). Further, comparative RNA-sequencing analysis using WT and Delta MoNdt80 revealed a large set of GlcNAc responsive genes that are under the transcriptional control of MoNdt80. These genes encoded GlcNAc catabolic enzymes, transporters and cell wall degrading enzymes which are required for hyphal growth expansion during host colonization. Overall, these results suggest MoNdt80 mediated transcriptional regulation of GlcNAc catabolic pathway is essential for successful host colonization and pathogenesis.

Safety of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Bhatt, DN; Ansari, S; Kumar, A; Ghosh, S; Narula, A; Datta, A 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

Shahnavaz, Z; Khaligh, NG; Zaharani, L; Johan, MR; Hamizi, NA in [Shahnavaz, Zohreh; Khaligh, Nader Ghaffari; Zaharani, Lia; Johan, Mohd Rafie; Hamizi, Nor Aliya] Univ Malaya, Nanotechnol & Catalysis Res Ctr, Inst Postgrad Studies, 3rd Floor,Block A, Kuala Lumpur 50603, Malaysia published The structure elucidation of new ionic liquid and its application for the synthesis of a series of novel triazolo[1,5-a]pyrimidine scaffolds in 2020.0, Cited 35.0. COA of Formula: C2H4N4. 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 present study, the chemical structure of 4,4′-trimethylene-N,N’-dipiperidinium chlorosulfonate is elucidated by 1D NMR, and 2D NMR, FTIR, Raman analyses, and Mass spectra. It was indicated that the chlorosulfonic acid could not act as a sulfonating agent in the reaction with secondary amines like TMDP due to due more steric hindrance of the sulfur atom by chlorine and oxygen atoms. Raman and FTIR spectra are demonstrated as two high-value optical techniques to the elucidation and identification of chemical structures that confirmed C3(v) symmetry for chlorosulfonate anion in the ionic liquid. Then, the solvent-catalyst activity of ionic liquid was demonstrated in the one-pot synthesis of a series of novel triazolo-pyrimidines under mild conditions. The ionic liquid was retrieved and reused several times without reducing its catalytic efficiency. (C) 2020 Elsevier B.V. All rights reserved.

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