550728
5-Aminotetrazole
97%
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About This Item
Produits recommandés
Pureté
97%
Pf
201-205 °C (lit.)
Chaîne SMILES
Nc1nnn[nH]1
InChI
1S/CH3N5/c2-1-3-5-6-4-1/h(H3,2,3,4,5,6)
Clé InChI
ULRPISSMEBPJLN-UHFFFAOYSA-N
Catégories apparentées
Description générale
5-Aminotetrazole (5-AT) can react with different 2-ethoxymethylidene-3-oxo esters and their analogs to form biologically important azaheterocycles.
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Aquatic Chronic 3 - Desen. Expl. 4 - Eye Dam. 1
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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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
High-Nitrogen-Based Pyrotechnics: Perchlorate-Free Red-and Green-Light Illuminants Based on 5-Aminotetrazole.
Chemistry (Weinheim An Der Bergstrasse, Germany), 19(38), 12839-12845 (2013)
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
Ionic liquid-promoted multicomponent synthesis of fused tetrazolo [1, 5-a] pyrimidines as a-glucosidase inhibitors.
Bioorganic & Medicinal Chemistry Letters, 26(16), 4007-4014 (2016)
Journal of molecular modeling, 14(5), 403-408 (2008-03-12)
The pathway and ab initio direct kinetics of the decomposition 5-aminotetrazole (5-ATZ) to HN(3) and NH(2)CN was investigated. Reactant, products and transition state were optimized with MP2 and B3LYP methods using 6-311G** and aug-cc-pVDZ basis sets. The intrinsic reaction coordinate
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