550728
5-Aminotetrazole
97%
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About This Item
Formula empirica (notazione di Hill):
CH3N5
Numero CAS:
Peso molecolare:
85.07
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
97%
Punto di fusione
201-205 °C (lit.)
Stringa SMILE
Nc1nnn[nH]1
InChI
1S/CH3N5/c2-1-3-5-6-4-1/h(H3,2,3,4,5,6)
ULRPISSMEBPJLN-UHFFFAOYSA-N
Descrizione generale
5-Aminotetrazole (5-AT) can react with different 2-ethoxymethylidene-3-oxo esters and their analogs to form biologically important azaheterocycles.
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Aquatic Chronic 3 - Desen. Expl. 4 - Eye Dam. 1
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
Certificati d'analisi (COA)
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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)
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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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