Triazoles

Authors Chhetri, S; Ghosh, S; Samanta, P; Murmu, NC; Kuila, T in WILEY-V C H VERLAG GMBH published article about FUNCTIONALIZED GRAPHENE; CORROSION PROTECTION; GRAPHITE OXIDE; ENHANCEMENT; RESISTANCE; NANOSHEETS; INHIBITORS; ZIRCONIA; DELIVERY; CATALYST in [Chhetri, Suman; Ghosh, Souvik; Samanta, Pranab; Murmu, Naresh Chandra; Kuila, Tapas] CSIR Cent Mech Enging Res Inst, Surface Engn & Tribol Div, Durgapur 713209, India; [Chhetri, Suman; Ghosh, Souvik; Samanta, Pranab; Murmu, Naresh Chandra; Kuila, Tapas] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India in 2019.0, Cited 41.0. Product Details of 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

The present study explores the synergistic effect of Fe3O4 and heteroatom doped reduced graphene oxide (rGO) nanohybrid on anti-corrosion performance of epoxy composite coating. In this connection, Fe3O4 nanoparticles were decorated over nitrogen doped rGO (Fe3O4-NRG) and characterized by Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray diffraction (XRD), X-ray Photoelectron spectroscopy (XPS), and Thermogravimetric analysis (TGA). This approach to modulating the surface properties of graphene and hence the interaction with polymer matrix were quite distinct from traditional surface functionlization or decoration in a sense that the doped nitrogen atom facilitate the growth of Fe3O4 particles and at the same time augmented the interaction of rGO with polymer matrix. The prepared nanohybrid was dispersed in epoxy matrix through mechanical mixing and coated over mild steel surface via spin coating technique. The potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) study revealed superior anti-corrosion performance of Fe3O4-NRG/epoxy coating in 3.5 wt% NaCl solution. The corrosion inhibition was found to improve by similar to 98.5% with 0.5 wt% loading of Fe3O4-NRG. We believe that this simple solvent free approach to prepare composite coating can be exploit for practical application and thus deserves special attention..

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Chhetri, S; Ghosh, S; Samanta, P; Murmu, NC; Kuila, T 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

HPLC of Formula: C2H4N4. Recently I am researching about NANOSHEETS; G-C3N4; NITROGEN; WATER; PERFORMANCE; EVOLUTION; TRANSFORMATIONS; MELAMINE; C3N4; SOFT, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21771061, 21601055]; University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2017118]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Zhao, C; Li, Q; Xie, Y; Zhang, LP; Xiao, XD; Wang, D; Jiao, YQ; Price, CAH; Jiang, BJ; Liu, J. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

The three-dimensional character of carbon nitride can endow it with a larger specific surface area and more catalytic active sites, which are beneficial for charge and mass transfer to enhance photocatalytic hydrogen production reactions. Herein, we reported the direct assembly of three-dimensional structured carbon nitride from the thermal polymerization of 3-amino-1,2,4-triazole (AT) and melamine molecules. The 3D C3N4 consisted of one-dimensional thick tubes with numbers of thin tubes grown uniformly on their surfaces. It was noted that the assembly was decorated with triazole ring groups that generated a special nitrogen-rich structure, further broadening the visible-light response range. Furthermore, the nitrogen-rich carbon nitride had a large surface area of 71 m(2) g(-1), leading to a significant increase in the number of catalytic active sites. Thus, the photocatalytic hydrogen production rate reached 7.1 mmol g(-1) h(-1), 11.2 times higher than that of bulk C3N4. This work may provide a new strategy to controllably synthesize three-dimensional carbon nitride assemblies for photocatalytic applications.

HPLC of Formula: C2H4N4. Welcome to talk about 61-82-5, If you have any questions, you can contact Zhao, C; Li, Q; Xie, Y; Zhang, LP; Xiao, XD; Wang, D; Jiao, YQ; Price, CAH; Jiang, BJ; Liu, J 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

Category: Triazoles. Recently I am researching about K+ CHANNELS; ANION; CHLORIDE; BINDING; SLIDES; TRANSPORTERS; RECEPTORS; RODS, Saw an article supported by the Agence Nationale de la RechercheFrench National Research Agency (ANR)European Commission [ANR-15-CE29-0009 DYNAFUN]; 1000 Talent Plan [WQ20144400255]; NSFC (National Natural Science Foundation of China), ChinaNational Natural Science Foundation of China (NSFC) [21720102007]; 111 project of SAFEA, China [90002-18011002]; China Scholarship CouncilChina Scholarship Council. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Zheng, SP; Li, YH; Jiang, JJ; van der Lee, A; Dumitrescu, D; Barboiu, M. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

The self-assembly of triazole amphiphiles was examined in solution, the solid state, and in bilayer membranes. Single-crystal X-ray diffraction experiments show that stacked protonated triazole quartets (T-4) are stabilized by multiple strong interactions with two anions. Hydrogen bonding/ion pairing of the anions are combined with anion-pi recognition to produce columnar architectures. In bilayer membranes, low transport activity is observed when the T-4 channels are operated as H+/X- translocators, but higher transport activity is observed for X- in the presence of the K+-carrier valinomycin. These self-assembled superstructures, presenting intriguing structural behaviors such as directionality, and strong anion encapsulation by hydrogen bonding supported by vicinal anion-pi interactions can serve as artificial supramolecular channels for transporting anions across lipid bilayer membranes.

Category: Triazoles. Welcome to talk about 61-82-5, If you have any questions, you can contact Zheng, SP; Li, YH; Jiang, JJ; van der Lee, A; Dumitrescu, D; Barboiu, M 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

Category: Triazoles. In 2020.0 BIOORG CHEM published article about BIOLOGICAL EVALUATION; TOPOISOMERASE-I; ANTICANCER; DESIGN; INHIBITORS; CHALCONES; ANALOGS; SERIES in [Radwan, Mohamed A. A.; Alshubramy, Maha A.; Abdel-Motaal, Marwa] Qassim Univ, Dept Chem, Collage Sci, Buraydah, Saudi Arabia; [Radwan, Mohamed A. A.] Natl Res Ctr, Dept Appl Organ Chem, Dokki, Egypt; [Abdel-Motaal, Marwa] El Mansoura Univ, Fac Sci, Dept Chem, Mansoura, Egypt; [Hemdan, Bahaa A.] Natl Res Ctr, Water Pollut Res Dept, Environm Microbiol Lab, 33 El Bohouth St, Giza 12622, Egypt; [El-Kady, Dina S.] Natl Res Ctr, Hormones Dept, Cairo, Egypt in 2020.0, Cited 56.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Synthesis of some new heterocyclic ring systems incorporated pyrimidine and pyridine moieties starting from 1-(furan-2-yl)-3-(thiophen-2-yl) chalcone was achieved. The structure of the new compounds was interpreted by spectral studies and ESI-MS analysis. Antimicrobial investigations of the designated compounds were performed towards some harmful pathogenic microbes. Antimicrobial tests proved that compound 11 unveiled a greater antimicrobial activity than other designed compounds. Docking of compound 11 into active site of DNA gyrase B chain displayed binding-energy of -13.05 kJ mol(-1) and distance at 3.18 A degrees. Furthermore, docking investigation was approved for the goal compounds into DNA gyrase B chain and exhibiting binding energy extended from -13.05 to -20.48 kJ mol(-1).

Welcome to talk about 61-82-5, If you have any questions, you can contact Radwan, MAA; Alshubramy, MA; Abdel-Motaal, M; Hemdan, BA; El-Kady, DS or send Email.. Category: Triazoles

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 of 1,2,4-triazolo[1,5-a]pyrimidine derivatives: Antimicrobial activity, DNA Gyrase inhibition and molecular docking WOS:000505596300067 published article about CATALYTIC INHIBITORS; DISCOVERY; DESIGN in [Abd El-Aleam, Rehab H.] Modern Univ Technol & Informat MTI, Fac Pharm, Pharmaceut Chem Dept, Cairo 11571, Egypt; [George, Riham F.; Hassan, Ghaneya S.] Cairo Univ, Fac Pharm, Pharmaceut Chem Dept, Cairo 11562, Egypt; [Hassan, Ghaneya S.] Badr Univ, Fac Pharm, Pharmaceut Chem Dept, Cairo 11829, Egypt; [Abdel-Rahman, Hamdy M.] Assiut Univ, Fac Pharm, Med Chem Dept, Assiut 71526, Egypt; [Abdel-Rahman, Hamdy M.] Nahda Univ, Fac Pharm, Pharmaceut Chem Dept, Bani Suwayf, Egypt in 2020.0, Cited 20.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Recommanded Product: 61-82-5

A series of 1,2,4-triazolo [1,5-a]pyrimidine derivatives was designed, synthesized and screened for their antibacterial and antifungal activities as well as their safety profile. Compounds 2b, 3a, 6b, 8b, 8c, 8h, 9a,b, 10b, 11a,b and 12a,b showed high activity against Gram-positive and Gram-negative bacteria with MIC values ranging from 0.25 to 2.0 mu g/mL. Many compounds were safe with no cytotoxicity against human embryonic kidney and red blood cells at concentration up to 32 mu g/mL. Moreover, compound 9a showed the highest inhibitory activity against DNA Gyrase with IC50 = 0.68 mu M compared to ciprofloxacin IC50 = 0.85 mu M. Molecular docking at DNA Gyrase active site revealed binding mode and docking scores comparable to that of ciprofloxacin confirming their antibacterial activity via DNA Gyrase inhibition.

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

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Recently I am researching about BINDING PROTEINS ZFP36L1; SECONDARY WALL FORMATION; WOOD FORMATION; GLUCURONOXYLAN BIOSYNTHESIS; TRANSCRIPTION FACTORS; CELL-PROLIFERATION; GENE-EXPRESSION; HD-ZIP; ARABIDOPSIS; GROWTH, Saw an article supported by the . Published in WILEY in HOBOKEN ,Authors: Tang, XF; Wang, D; Liu, Y; Lu, MZ; Zhuang, YM; Xie, Z; Wang, CP; Wang, SM; Kong, YZ; Chai, GH; Zhou, GK. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Wood (secondary xylem) formation in tree species is dependent on auxin-mediated vascular cambium activity in stems. However, the complex regulatory networks underlying xylem formation remain elusive. Xylem development in Populus was characterized based on microscopic observations of stem sections in transgenic plants. Transcriptomic, quantitative real-time PCR, chromatin immunoprecipitation PCR, and electrophoretic mobility shift assay analyses were conducted to identify target genes involved in xylem development. Yeast two-hybrid, pull-down, bimolecular fluorescence complementation, and co-immunoprecipitation assays were used to validate protein-protein interactions. PaC3H17 and its target PaMYB199 were found to be predominantly expressed in the vascular cambium and developing secondary xylem in Populus stems and play opposite roles in controlling cambial cell proliferation and secondary cell wall thickening through an overlapping pathway. Further, PaC3H17 interacts with PaMYB199 to form a complex, attenuating PaMYB199-driven suppression of its xylem targets. Exogenous auxin application enhances the dual control of the PaC3H17-PaMYB199 module during cambium division, thereby promoting secondary cell wall deposition. Dual regulation of xylem formation by an auxin-mediated PaC3H17-PaMYB199 module represents a novel regulatory mechanism in Populus, increasing our understanding of the regulatory networks involved in wood formation.

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 Tang, XF; Wang, D; Liu, Y; Lu, MZ; Zhuang, YM; Xie, Z; Wang, CP; Wang, SM; Kong, YZ; Chai, GH; Zhou, GK 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

I found the field of Chemistry; Science & Technology – Other Topics; Engineering very interesting. Saw the article Facile Covalent Crosslinking of Zeolitic Imidazolate Framework/Polydimethylsiloxane Mixed Matrix Membrane for Enhanced Ethanol/Water Separation Performance published in 2020.0. Name: 1H-1,2,4-Triazol-5-amine, Reprint Addresses Wang, Y (corresponding author), Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Minist Educ, Key Lab Mat Chem Energy Convers & Storage, Wuhan 430074, Peoples R China.; Wang, Y (corresponding author), Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

The interfacial design is critical in preparing high-performance mixed matrix membranes (MMMs), especially for the separation of larger sized components from mixtures. Herein, a facile and novel strategy was employed to design covalently linked zeolitic imidazolate framework-8-polydimethylsiloxane (ZIF-8@PDMS) MMMs without interfacial defects by a onestep synthesis route for ethanol recovery from ethanol aqueous solution. In this strategy, 3-glycidyloxypropyltrimethoxysilane (GOPTS) worked as the covalent linker of PDMS and amine-functionalized ZIF-8 nanoparticles (AZIF-8) simultaneously. The chemical structures and morphologies of AZIF-8 and AZIF-8@PDMS MMMs were demonstrated by various characterization techniques. The results exhibited that AZIF-8 and the MMMs were successfully prepared and AZIF-8 as the filler displayed better dispersion in the PDMS matrix and compatibility with the PDMS matrix as compared to ZIF-8 or GOPTS-modified ZIF-8 (GZIF-8). Therefore, AZIF-8@PDMS MMMs showed more excellent separation performance than ZIF-8 or GZIF-8-filled MMMs. In particular, AZIF-8@PDMS MMM with 7 wt % AZIF-8 loading exhibited the highest separation factor of 17.7 and a comparable total flux of 585.6 g/m(2) h at 40 degrees C with 5 wt % ethanol aqueous solution, which were improved by 176.6 and 34.5%, respectively, in comparison with the pristine PDMS membrane, breaking the trade-off effect between the flux and separation factor. This study might provide some new insights into the fabrication of high-performance MMMs for pervaporation recovery of various organic systems.

Welcome to talk about 61-82-5, If you have any questions, you can contact Zhu, TY; Yu, X; Yi, M; Wang, Y or send Email.. Name: 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

HPLC of Formula: C2H4N4. In 2020.0 BIOORG MED CHEM LETT published article about ACID-DERIVATIVES; TRIAZOLE in [Safari, Fatemeh] Univ Guilan, Fac Sci, Dept Biol, Rasht, Iran; [Bayat, Mohammad; Nasri, Shima; Karami, Solmaz] Imam Khomeini Int Univ, Fac Sci, Dept Chem, Qazvin, Iran in 2020.0, Cited 25.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Cancer is a leading cause of human death worldwide. One of the greatest challenges in cancer therapy is the discovery and design of novel products with potential anti-tumor activities. In this study, a new protocol involves three-component condensation of the 3-amino-1,2,4-triazole as a 1,3-binucleophile, versatile aldehydes and Nmethyl-1-(methylthio)-2-nitroethenamine as an enamine analogous in the presence of trichloroacetic acid as a Bronsted-Lowry acidic promoter leads to new functionalized N-alkyl-6-nitro-3,5-dihydro-[1,2,4]triazolo [1,5-a] pyrimidin-7-amine in moderate to good yields. The presence of five nitrogen heteroatoms in the product structure has gathered immense attention among chemists and biologists due to their biological values. Therefore, we evaluated the anti-tumor activity of our synthetic compounds on different cancer cells including human malignant melanoma cells (A375), prostate cancer cells (PC3 cells, LNCaP cells) and normal cells HDF (human dermal fibroblast). Notably, we found that compound 4b that contains a nitro group has the best antitumor activity on three different cancer cells. By using DAPI staining, we showed cancer cells death. Apoptosis induction was shown using quantitative real time PCR (qRT-PCR) by evaluating of Bax and Bcl2 mRNA levels. Finally, we demonstrated that 4b has epithelial-to-mesenchymal transition (EMT) inhibition effect on cancer cells (by induction of E-cadherin and reduction of vimentin mRNA expression levels as two potential EMT markers). So, 4b could be an anti-cancer promising drug. Although, in vivo experiments will be required to evaluate possible side effects.

HPLC 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

I found the field of Pharmacology & Pharmacy very interesting. Saw the article A multifunctional therapeutic approach: Synthesis, biological evaluation, crystal structure and molecular docking of diversified 1H-pyrazolo[3,4-b]pyridine derivatives against Alzheimer’s disease published in 2019.0. Safety of 1H-1,2,4-Triazol-5-amine, Reprint Addresses Hoda, N (corresponding author), Jamia Millia Islamia, Dept Chem, New Delhi 110025, India.; Tiwari, M (corresponding author), Univ Delhi, Dr BR Ambedkar Ctr Biomed Res, New Delhi 110007, India.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

2-(piperazin-1-yl)-N-(1H-pyrazolo[3,4-b]pyridin-3-yl)acetamides are described as a new class of selective and potent acetylcholinesterase (AChE) inhibitors and amyloid beta aggregation inhibitors. Formation of synthesized compounds (P1-P9) was justified via H-1 NMR, C-13 NMR, mass spectra and single crystal X-Ray diffraction study. All compounds were evaluated for their acetylcholinesterase and butyrylcholinesterase inhibitory activity, inhibition of self-mediated A beta aggregation and Cu(II)-mediated A beta aggregation. Also, docking study carried out was in concordance with in vitro results. The most potent molecule amongst the derivatives exhibited excellent anti-AChE activity (IC50=4.8 nM). Kinetic study of P3 suggested it to be a mixed type inhibitor. In vitro study revealed that all the compounds are capable of inhibiting self-induced beta-amyloid (A beta) aggregation with the highest inhibition percentage to be 81.65%. Potency of P1 and P3 to inhibit self-induced A beta(1-)(42) aggregation was ascertained by TEM analysis. Compounds were also evaluated for their A beta disaggregation, antioxidation, metal-chelation activity. (C) 2019 Elsevier Masson SAS. All rights reserved.

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.. Safety 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

Recommanded Product: 1H-1,2,4-Triazol-5-amine. Authors Yildirim, C; Ozkaya, B; Bal, R in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Yildirim, Caner; Ozkaya, Beytullah; Bal, Ramazan] Gaziantep Univ, Fac Med, Dept Physiol, TR-27310 Gaziantep, Turkey in 2021.0, Cited 100.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

ATP-sensitive potassium (K-ATP) channels and transient receptor potential melastatin 2 (TRPM2) channels are commonly expressed both pre- and postsynaptically in the central nervous system (CNS). We hypothesized that K-ATP and TRPM2 may couple metabolic status to the resting membrane potential of octopus neurons of the mouse ventral cochlear nucleus (VCN). Therefore, we studied the expression of K-ATP channels and TRPM2 channels in octopus cells by immunohistochemical techniques and their contribution to neuronal electrical properties by the electrophysiological patch clamp technique. In immunohistochemical staining of octopus cells, labelling with Kir6.2 and SUR1 antibodies was strong, and labelling with the SUR2 antibody was moderate, but labelling with Kir6.1 was very weak. Octopus cells had intense staining with TRPM2 antibodies. In patch clamp recordings, bath application of KATP channel agonists H2O2 (880 mu M), ATZ (1 mM), cromakalim (50 mu M), diazoxide (200 mu M), NNC 55-0118 and NN 414 separately resulted in hyperpolarizations of resting potential to different extents. Application of 8-Bro-cADPR (50 mu M), a specific antagonist of TRPM2 channels, in the presence of H2O2 (880 mu M) resulted in further hyperpolarization by approximately 1 mV. The amplitudes of H2O2-induced outward K-ATP currents and ADPR-induced inward currents were 206.1 +/- 31.5 pA (n = 4) and 136.8 +/- 22.4 pA, respectively, at rest. Their respective reversal potentials were -77 +/- 2.6 mV (n = 3) and -6.3 +/- 2.9 (n = 3) and -6.3 +/- 2.9 (n = 3). In conclusion, octopus cells appear to possess both K-ATP channels and TRPM2-like channels. K-ATP might largely be constituted by SUR1-Kir6.2 subunits and SUR2-Kir6.2 subunits. Both K-ATP and TRPM2-like channels might have a modulatory action in setting the membrane potential.

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