550728
5-Aminotetrazole
97%
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About This Item
Formule empirique (notation de Hill):
CH3N5
Numéro CAS:
Poids moléculaire :
85.07
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
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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An efficient synthesis of tetrahydrotetrazolo [1, 5-a] quinazoline derivatives by a three-component reaction of 5-aminotetrazole, arylaldehydes, and dimedone.
Hassankhani A and Mosaddegh E.
Scientia Iranica. Transaction C, Chemistry, Chemical Engineering, 22(3), 942-942 (2015)
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
S Thomas et al.
The journal of physical chemistry. A, 109(44), 9928-9934 (2006-07-15)
The surface-enhanced Raman scattering (SERS) studies of 5-amino tetrazole (5AT), a tetrazole derivative, in aqueous silver sol at pH approximately 9 and on deposited colloidal silver films were carried out and compared with the normal Raman spectrum of the molecule.
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
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
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