What unique challenges do researchers face in 61-82-5

Welcome to talk about 61-82-5, If you have any questions, you can contact Yildirim, C; Ozkaya, B; Bal, R or send Email.. Product Details of 61-82-5

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. 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

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.

Welcome to talk about 61-82-5, If you have any questions, you can contact Yildirim, C; Ozkaya, B; Bal, R or send Email.. 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

Our Top Choice Compound:1H-1,2,4-Triazol-5-amine

Welcome to talk about 61-82-5, If you have any questions, you can contact Lauar, MR; Colombari, DSA; Colombari, E; De Paula, PM; De Luca, LA; Menani, JV or send Email.. HPLC of Formula: C2H4N4

Lauar, MR; Colombari, DSA; Colombari, E; De Paula, PM; De Luca, LA; Menani, JV in [Lauar, Mariana R.; Colombari, Debora S. A.; Colombari, Eduardo; De Paula, Patricia M.; De Luca Jr, Laurival A.; Menani, Jose, V] Sao Paulo State Univ UNESP, Dent Sch, Dept Physiol & Pathol, Araraquara, SP, Brazil published Catalase blockade reduces the pressor response to central cholinergic activation in 2019.0, Cited 66.0. HPLC 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.

Intracerebroventricular (icv) injection of hydrogen peroxide (H2O2), a reactive oxygen species, or the blockade of catalase (enzyme that degrades H2O2 into H2O and O-2) with icv injection of 3-amino-1,2,4-triazole (ATZ) reduces the pressor effects of angiotensin II also injected icv. In the present study, we investigated the effects of ATZ injected icv or intravenously (iv) on the pressor responses induced by icv injections of the cholinergic agonist carbachol, which similar to angiotensin II induces pressor responses that depend on sympathoexcitation and vasopressin release. In addition, the effects of H2O2 icv on the pressor responses to icv carbachol were also tested to compare with the effects of ATZ. Normotensive non-anesthetized male Holtzman rats (280-300 g, n = 8-9/group) with stainless steel cannulas implanted in the lateral ventricle were used. Previous injection of ATZ (5 nmol/1 mu l) or H2O2 (5 mu mol/1 mu l) icv similarly reduced the pressor responses induced by carbachol (4 nmol/1 mu l) injected icv (13 +/- 4 and 12 +/- 4 mmHg, respectively, vs. vehicle + carbachol: 30 +/- 5 mmHg). ATZ (3.6 mmol/kg of body weight) injected iv also reduced icv carbachol-induced pressor responses (21 +/- 2 mmHg). ATZ icv or iv and H2O2 icv injected alone produced no effect on baseline arterial pressure. The treatments also produced no significant change of heart rate. The results show that ATZ icv or iv reduced the pressor responses to icv carbachol, suggesting that endogenous H2O2 acting centrally inhibits the pressor mechanisms (sympathoactivation and/or vasopressin release) activated by central cholinergic stimulation.

Welcome to talk about 61-82-5, If you have any questions, you can contact Lauar, MR; Colombari, DSA; Colombari, E; De Paula, PM; De Luca, LA; Menani, JV or send Email.. 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

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SDS of cas: 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.

I found the field of Chemistry; Energy & Fuels; Materials Science very interesting. Saw the article Three-dimensional assemblies of carbon nitride tubes as nanoreactors for enhanced photocatalytic hydrogen production published in 2020.0. SDS of cas: 61-82-5, Reprint Addresses Jiang, BJ (corresponding author), Heilongjiang Univ, Sch Chem & Mat Sci, Minist Educ Peoples Republ China, Key Lab Funct Inorgan Mat Chem, Harbin 150080, Heilongjiang, Peoples R China.; Liu, J (corresponding author), Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, 457 Zhongshan Rd, Dalian 116023, Peoples R China.; Liu, J (corresponding author), Univ Surrey, Dept Chem & Proc Engn, DICP Surrey Joint Ctr Future Mat, Guildford, Surrey, England.. 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.

SDS of cas: 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

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Formula: C2H4N4. 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.

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. Formula: C2H4N4, 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.

Formula: C2H4N4. 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

Can You Really Do Chemisty Experiments About 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.. COA of Formula: C2H4N4

Recently I am researching about CYTOTOXIC ACTIVITY; DERIVATIVES, Saw an article supported by the Natural Science Foundation of Shaanxi Province of ChinaNatural Science Foundation of Shaanxi Province [2018JQ2033]; Key Research and Development Project of Shaanxi Province of China [2018ZDXM-NY-064]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21402156]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Fan, NJ; Tang, JJ; Li, YF; Bai, YB; Zhao, XM. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. COA of Formula: C2H4N4

A facile strategy for the synthesis of steroidal [1,2,4]triazolo[1,5-a]pyrimidines 5a-g and 6a-g has been accomplished via a one-pot reaction of steroidal ketones, aromatic aldehydes and 3-amino-1,2,4-triazole in the presence of potassium tert-butoxide in refluxing tert-butanol. All the synthesized heterosteroids were evaluated for in vitro antiproliferative activity against human cancer cells by sulforhodamine B (SRB) assays. The preliminary results showed that compounds 6a and 6e possessed potent antiproliferative activities.

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

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Name: 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Akrami, S; Karami, B; Farahi, M or send Email.

Name: 1H-1,2,4-Triazol-5-amine. Akrami, S; Karami, B; Farahi, M in [Akrami, Sedigheh; Karami, Bahador; Farahi, Mahnaz] Univ Yasuj, Dept Chem, Yasuj 7591874831, Iran published A novel protocol for catalyst-free synthesis of fused six-member rings to triazole and pyrazole in 2020.0, 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.

Herein, an effectual, quick and novel method is described for the synthesis of new triazolo[1,5-a]pyrimidine, triazolo[5,1-b][1,3] thiazine and pyrazolo[1,5-a]pyrimidine derivatives. This series of fused six-member rings to triazole and pyrazole was prepared via the catalyst-free reaction of dialkyl acetylenedicarboxylates and 3-substituted 1H-1,2,4-triazole or 3-amino-1H-pyrazole-4-carbonitrile. The structures of the prepared products were deduced from their Fourier-transform infrared, elemental analysis and proton and carbon-13 nuclear magnetic resonance spectral data. Graphical abstract A novel and green method is described for the synthesis of new triazolo[1,5-a]pyrimidine, triazolo[5,1-b][1,3] thiazine and pyrazolo[1,5-a]pyrimidine derivatives. [GRAPHICS] .

Name: 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Akrami, S; Karami, B; Farahi, 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

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Recommanded Product: 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Yu, WW; Shan, X; Zhao, ZK or send Email.

An article Unique nitrogen-deficient carbon nitride homojunction prepared by a facile inserting-removing strategy as an efficient photocatalyst for visible light-driven hydrogen evolution WOS:000532683200036 published article about IN-SITU CONSTRUCTION; SURFACE-AREA; G-C3N4; DEFECTS; WATER; FABRICATION; NANOSHEETS; HETEROJUNCTIONS; COMPOSITES; CATALYST in [Yu, Weiwei; Shan, Xin; Zhao, Zhongkui] Dalian Univ Technol, PSU DUT Joint Ctr Energy Res, Sch Chem Engn, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China 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. Recommanded Product: 1H-1,2,4-Triazol-5-amine

Efficiently improving photocatalytic efficiency of carbon nitride (g-C3N4), a pro-mising candidate, for H-2 production is of great significance but remains a challenge. Herein, a unique N-deficient g-C3N4 homojunction (I/R-CN) prepared by an inserting-removing strategy via thermal polymerization of a freeze-dried mixture containing dicyandiamide, NH4Cl, and a prepolymer from 3-amino-1,2,4-triazol (3-AT) is reported, in which the prepolymerization process of 3-AT under optimized conditions is indispensible. I/R-CN features the N-deficient gC(3)N(4) microdomains (NDMD) from prepolymer inserting into a porous N-defects modified g-C3N4 with two kinds of N defects (N vacancies and cyano groups) formed by removing N atoms from the skeleton of g-C3N4, unambiguously confirmed by various characterizations. I/R-CN exhibits notably promoted photocatalysis with a high H-2 evolution rate of 3882.5 mu mol h(-1) g(-1) and a large apparent quantum yield of 8.6 % at 420 nm, originating from the efficient recombination inhibition of electron-hole pairs by the markedly promoted charge mobility as well as the improved light absorption capacity and enlarged reduction potential. This work paves a new avenue for designing other highly-efficient carbon nitride photocatalysts for solar applications.

Recommanded Product: 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Yu, WW; Shan, X; Zhao, ZK 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

Extended knowledge of 1H-1,2,4-Triazol-5-amine

Recommanded Product: 61-82-5. Welcome to talk about 61-82-5, If you have any questions, you can contact Fahim, AM; Farag, AM or send Email.

An article Synthesis, antimicrobial evaluation, molecular docking and theoretical calculations of novel pyrazolo[1,5-a]pyrimidine derivatives WOS:000492858500104 published article about BIOLOGICAL EVALUATION; EQUILIBRIUM GEOMETRIES; TOPOLOGICAL PROPERTIES; VIBRATIONAL-SPECTRA; CRYSTAL-STRUCTURE; FT-RAMAN; DFT; INHIBITORS; MECHANISM; TOOL in [Fahim, Asmaa M.] Natl Res Ctr Dokki, Green Chem Dept, POB 12622, Cairo, Egypt; [Farag, Ahmad M.] Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt in 2020.0, Cited 66.0. 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

New fused heterocyclic compounds were synthesized starting from dimethyl terephthalate, as a versatile precursor, via its reactions with the appropriate reagents. The structures of the newly synthesized compounds were supported by their spectral data. Some of the newly synthesized compounds exhibited promising antimicrobial activities. Molecular docking studies were carried out on 4-(5-amino-7-(4-bromophenyl)pyrazolo[1,5-a]pyrimidine-6-carbonyl) benzoic acid (17) as the most active compound to evaluate its potential interaction molecular docking against Escherichia coli (PDB.ID: 3t88), StReptococcus pneumoniae (PDB.ID: 2wje), Asperglllus flavus (PDB.ID: 4ynt) and Geotrichum candidum (PDB.ID: 1tgh), respectively. Computational calculations at the DFT/B3LYP/6-31G (d) and HF/6-31G (d) level of the theory have been carried out to examine the equilibrium geometry of the pyrazolo[1,5-a]pyrimidine and harmonic vibrational frequencies, The energy of the HOMO and LUMO and Mullikan atomic charges were also calculated. (C) 2019 Published by Elsevier B.V.

Recommanded Product: 61-82-5. Welcome to talk about 61-82-5, If you have any questions, you can contact Fahim, AM; Farag, AM 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

Our Top Choice Compound:1H-1,2,4-Triazol-5-amine

Welcome to talk about 61-82-5, If you have any questions, you can contact Kiss, MA; Perina, M; Bazgier, V; May, NV; Baji, A; Jorda, R; Frank, E or send Email.. Category: Triazoles

Recently I am researching about GALETERONE; DEGRADATION; ABIRATERONE; INHIBITION; CHROMATIN; ESTRONE; BINDING; ACCESS, Saw an article supported by the National Research, Development and Innovation OfficeNational Research, Development & Innovation Office (NRDIO) – Hungary [OTKA K124544]; Grant Agency of the Czech RepublicGrant Agency of the Czech Republic [GA20-15621S]; Palacky University Olomouc [IGA_PrF_2021_007]; ELIXIR CZ research infrastructure project (MEYS) [LM2018131]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Kiss, MA; Perina, M; Bazgier, V; May, NV; Baji, A; Jorda, R; Frank, E. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Category: Triazoles

One of the main directions of steroid research is the preparation of modified derivatives in which, in addition to changes in physicochemical properties, receptor binding is significantly altered, thus a bioactivity different from that of the parent compound predominates. In the frame of this work, 2-arylidene derivatives were first synthesized by regioselective modification of the A-ring of natural sex hormone, 5 alpha-dihydrotestosterone (DHT). After Claisen-Schmidt condensations of DHT with (hetero)aromatic aldehydes in alkaline EtOH, heterocyclizations of the alpha,beta-enones were performed with 3-amino-1,2,4-triazole, 3-aminopyrazole and 3-amino-5-methylpyrazole in the presence of t-BuOK in DMF to afford 7 ‘-epimeric mixtures of A-ring-fused azolo-dihydropyrimidines, respectively. Depending on the electronic demand of the substituents of the arylidene moiety, spontaneous or 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ)-induced oxidation of the heteroring led to triazolo[1,5-a]pyrimidines and pyrazolo[1,5-a]pyrimidines in good yields, while, using the Jones reagent as a strong oxidant, 17oxidation also occurred. The crystal structures of an arylidene and a triazolopyrimidine product have been determined by single crystal X-ray diffraction and both were found to crystallize in the monoclinic crystal system at P21 space group. Most derivatives were found to diminish the transcriptional activity of androgen receptor (AR) in reporter cell line. The candidate compound (17 beta-hydroxy-2-(4-chloro)benzylidene-5 alpha-androstan-3-one, 2f) showed to suppress androgen-mediated AR transactivation in a dose-dependent manner. We confirmed the cellular interaction of 2f with AR, described the binding in AR-binding cavity by the flexible docking and showed the ability of the compound to suppress the expression of AR-regulated genes in two prostate cancer cell lines.

Welcome to talk about 61-82-5, If you have any questions, you can contact Kiss, MA; Perina, M; Bazgier, V; May, NV; Baji, A; Jorda, R; Frank, E 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

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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.. Computed Properties of C2H4N4

An article An insoluble naphthalenediimide derivative as a highly stable cathode material for lithium-ion batteries WOS:000484645900048 published article about ENERGY-STORAGE; ELECTROCHEMICAL PROPERTIES; POLYMER; ELECTRODES; CAPACITY; PERFORMANCE; CARBONYL; MOLECULES; COMPOUND in [Sun, Guangchi; Sha, Yanyong; Shi, Changdong; Zhang, Hanping; Liu, Qi] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, 1 Gehu Rd, Changzhou 213164, Jiangsu, Peoples R China; [Sun, Guangchi; Sha, Yanyong; Shi, Changdong; Zhang, Hanping; Liu, Qi] Changzhou Univ, Jiangsu Prov Key Lab Fine Petrochem Engn, 1 Gehu Rd, Changzhou 213164, Jiangsu, Peoples R China; [Hu, Yao; Liu, Hong-Jiang] Shanghai Univ, Coll Sci, Dept Chem, 99 Shangda Rd, Shanghai 200444, Peoples R China; [Yin, Gui; Liu, Qi] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China in 2019.0, Cited 58.0. Computed Properties of 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 new naphthalenediimide derivative, 2, 7-di (1, 2, 4-triazolyl) benzophenanthroline-tetraone (3-DTBPT) is synthesized by the condensation reaction of 1, 4, 5, 8-naphthalenetetracarboxylic anhydride (NTCDA) and 3-amino-1, 2, 4-triazole (3-AT). The 3-DTBPT material is characterized by Fourier transform infrared spectrum, X-ray diffraction, thermogravimetric analysis, solid state NMR spectra, field emission scanning electron microscopy, elemental analysis and Brunauer-Emmett-Teller surface. 3-DTBPT is insoluble in organic electrolyte. When used as a cathode material of lithium-ion batteries, 3-DTBPT exhibits an excellent cyclic stability, keeping a specific capacity of 110 mA h g(-1) and a nearly 94.8% capacity retention after 50 cycles at 50 mA g(-1). Our work provides an effective route for overcoming the dissolution problem of organic electrode materials and obtains a potential material for the long-cycle-life and flexible organic rechargeable batteries.

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.. 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