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Merck
CN

550728

5-氨基四氮唑

97%

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经验公式(希尔记法):
CH3N5
化学文摘社编号:
分子量:
85.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
224-581-7
MDL number:
Assay:
97%
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InChI key

ULRPISSMEBPJLN-UHFFFAOYSA-N

InChI

1S/CH3N5/c2-1-3-5-6-4-1/h(H3,2,3,4,5,6)

SMILES string

Nc1nnn[nH]1

assay

97%

mp

201-205 °C (lit.)

General description

5-Aminotetrazole (5-AT) can react with different 2-ethoxymethylidene-3-oxo esters and their analogs to form biologically important azaheterocycles.

pictograms

FlameCorrosion

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Desen. Expl. 4 - Eye Dam. 1

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

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W C de Bruijn et al.
The Histochemical journal, 16(1), 37-50 (1984-01-01)
Addition of heterocyclic nitrogen compounds to the classical osmium tetroxide postfixation medium, applied after glutaraldehyde fixation, results in enhanced membrane contrast in ultrathin sections of liver tissue. The addition of similar compounds to potassium osmate solutions, results in contrast differences
High-Nitrogen-Based Pyrotechnics: Perchlorate-Free Red-and Green-Light Illuminants Based on 5-Aminotetrazole.
Sabatini JJ and Moretti JD.
Chemistry (Weinheim An Der Bergstrasse, Germany), 19(38), 12839-12845 (2013)
Jian-Guo Zhang et al.
Journal of molecular modeling, 15(1), 67-77 (2008-10-23)
The tautomerism and intramolecular hydrogen shifts of 5-amino-tetrazole in the gas phase were studied in the present work. The minimum energy path (MEP) information of 5-amino-tetrazole was obtained at the CCSD(T)/6-311G**//MP2/6-311G** level of theory. The six possible tautomers of 1H
Selda Abyar et al.
Scientific reports, 9(1), 14686-14686 (2019-10-13)
Complexes based on heavy metals have great potential for the treatment of a wide variety of cancers but their use is often limited due to toxic side effects. Here we describe the synthesis of two new cadmium complexes using N(4)-phenyl-2-formylpyridine
Ionic liquid-promoted multicomponent synthesis of fused tetrazolo [1, 5-a] pyrimidines as a-glucosidase inhibitors.
Suresh L, et al.
Bioorganic & Medicinal Chemistry Letters, 26(16), 4007-4014 (2016)

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