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550728

Sigma-Aldrich

5-Aminotetrazol

97%

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About This Item

Empirische Formel (Hill-System):
CH3N5
CAS-Nummer:
4418-61-5
Molekulargewicht:
85.07
EG-Nummer:
224-581-7
MDL-Nummer:
MFCD00005248
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24879141
NACRES:
NA.22

Assay

97%

mp (Schmelzpunkt)

201-205 °C (lit.)

SMILES String

Nc1nnn[nH]1

InChI

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

InChIKey

ULRPISSMEBPJLN-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

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

Piktogramme

FlameCorrosion
GHS02,GHS05

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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1,2,4-Triazol 98%

Sigma-Aldrich

T46108

1,2,4-Triazol

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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