Imidazole-2-carboxaldehyde

Imidazole-2-carboxaldehyde Basic information

Product Name:	Imidazole-2-carboxaldehyde
Synonyms:	2-FORMAYLIMIDAZOLE;Imidazole-2-carboxaldehyde p;Imidazole-2-carboxaldehyde ,98%;Imidazole-2-carboxal;2-AcetliMidazole;2-Formyl-1H-imidazole;2-IMidazolecarboxaldehyde 97%;Imidazole-2-carboxaldehyde,97%
CAS:	10111-08-7
MF:	C4H4N2O
MW:	96.09
EINECS:	600-165-4
Product Categories:	Imidazoles & Benzimidazoles;Building Blocks;Heterocyclic Building Blocks;Imidazole;Imidazol&Benzimidazole;Imidaxoles;Building Blocks;C1 to C6;Carbonyl Compounds;Chemical Synthesis;Heterocyclic Building Blocks;Organic Building Blocks;Aldehydes;blocks;Imidazoles;Imidazoles & Benzimidazoles
Mol File:	10111-08-7.mol

Imidazole-2-carboxaldehyde Chemical Properties

Melting point	209 °C (dec.) (lit.)
Boiling point	296.5±23.0 °C(Predicted)
density	1.322±0.06 g/cm3(Predicted)
storage temp.	Keep in dark place,Inert atmosphere,Room temperature
solubility	DMSO (Sparingly), Methanol (Slightly, Sonicated)
form	Solid
pka	11.48±0.10(Predicted)
color	Light Brown to Brown
Water Solubility	Soluble in water.
Sensitive	Air Sensitive
BRN	4371302
InChIKey	XYHKNCXZYYTLRG-UHFFFAOYSA-N
CAS DataBase Reference	10111-08-7(CAS DataBase Reference)
NIST Chemistry Reference	1H-imidazole-2-carboxaldehyde(10111-08-7)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36-36/37/39-3
WGK Germany	3
F	10
HazardClass	IRRITANT
HS Code	29332900

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

Imidazole-2-carboxaldehyde Usage And Synthesis

Chemical Properties	White to light brown solid
Uses	1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
Uses	Used in a study of the imidazole-directed allylation of aldimines.1
Uses	Imidazole-2-carboxaldehyde is a novel protein tyrosine phosphatase 1B (PTP1B) inhibitor with an important application to treat type-2 diabetes. It is used in the preparation of tridentate Schiff-base carboxylate-containing ligands by undergoing condensation reaction with amino acids beta-alanine and 2-aminobenzoic acid. It is also involved in the study of the imidazole-directed allylation of aldimines.
Synthesis Reference(s)	Organic Syntheses, Coll. Vol. 7, p. 287, 1990 The Journal of Organic Chemistry, 60, p. 1090, 1995 DOI: 10.1021/jo00109a052

Imidazole-2-carboxaldehyde Preparation Products And Raw materials

Raw materials	Hydrochloric acid-->n-Butyllithium-->Formaldehyde-->Diethylamine-->Imidazole-->Methyl formate-->1-TRITYLIMIDAZOLE-2-CARBOXALDEHYDE-->2-Bromo-1H-imidazole
Preparation Products	(1H-IMIDAZOL-2-YL)-METHANOL-->(1H-IMIDAZOL-2-YLMETHYL)-METHYL-AMINE-->Hexamethylenediamine-->2-Methylimidazole-->3-Amino-9-ethylcarbazole-->1H-Imidazole-2-carboxylic acid

IMIDAZO[1,2-B]ISOQUINOLINE-5,10-DIONE 2-Acetylbenzimidazole 1-(4-CHLOROBENZYL)-1H-BENZIMIDAZOLE-2-CARBALDEHYDE 4-Fluorobenzimidazole-2-carboxylic acid Ethanone, 1-(1-methyl-1H-benzimidazol-2-yl)- (9CI) N-phenyl-1H-imidazole-2-carboxamide 2-Benzimidazolecarboxylic acid (1H-IMIDAZOL-2-YL)-PHENYL-METHANONE Imidazole-2-carboxaldehyde, 1-benzyl- 6H,13H-PYRAZINO[1,2-A:4,5-A']BISBENZIMIDAZOLE-6,13-DIONE 2-(2-FUROYL)-4(5)-(2-FURANYL)-1H-IMIDAZOLE (4-CHLOROPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANONE 1H-BENZOIMIDAZOLE-2-CARBOXYLIC ACID ETHYL ESTER (2-chlorophenyl)(1H-imidazol-2-yl)methanone 1H-Benzimidazole-2-carboxaldehyde 1-METHYL-5-NITRO-1H-IMIDAZOLE-2-CARBALDEHYDE AKOS BBS-00002808 AKOS BBS-00002810

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