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164968

Sigma-Aldrich

5-Amino-4-imidazolecarboxamide hydrochloride

98%

Synonym(s):

4-Amino-5-imidazolecarboxamide hydrochloride, AICA

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About This Item

Empirical Formula (Hill Notation):
C4H6N4O · HCl
CAS Number:
Molecular Weight:
162.58
Beilstein/REAXYS Number:
3701645
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

powder

mp

250-252 °C (dec.) (lit.)

solubility

water: soluble 50 mg/mL, clear, light yellow

functional group

amide

SMILES string

Cl[H].NC(=O)c1[nH]cnc1N

InChI

1S/C4H6N4O.ClH/c5-3-2(4(6)9)7-1-8-3;/h1H,5H2,(H2,6,9)(H,7,8);1H

InChI key

MXCUYSMIELHIQL-UHFFFAOYSA-N

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General description

Corrosion inhibition and adsorption characteristics of 5-amino-4-imidazolecarboxamide hydrochloride on aluminum in 1M HCl has been investigated.

Application

5-Amino-4-imidazolecarboxamide hydrochloride was used in the synthesis of heterocyclic compounds such as guanine, purines and pyrimidines.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Journal of Heterocyclic Chemistry, 30, 593-593 (1993)
Heterocycles, 34, 1133-1133 (1992)
The Journal of Organic Chemistry, 56, 2139-2139 (1991)
Fang Li et al.
Scientific reports, 6, 37114-37114 (2016-11-22)
GRS is a drug combination of three active components including ginsenoside Rb1, ruscogenin and schisandrin. It derived from the well-known TCM formula ShengMai preparations, a widely used traditional Chinese medicine for the treatment of cardiovascular diseases in clinic. The present
Synthesis of guanosine and its derivatives from 5-amino-1-beta-d-ribofuranoxyl-4-imidazolecarboxamide. I. Ring closure with benzoyl isothiocyanate.
A Yamazaki et al.
The Journal of organic chemistry, 32(6), 1825-1828 (1967-06-01)

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