Cas 108403-90-3,3-Benzyl-2-(4-chloro-2-nitro-phenylsulfanyl)-3H-imidazole-4-carboxylic acid

108403-90-3

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Basic information

Product Name: 3-Benzyl-2-(4-chloro-2-nitro-phenylsulfanyl)-3H-imidazole-4-carboxylic acid
Synonyms: 3-Benzyl-2-(4-chloro-2-nitro-phenylsulfanyl)-3H-imidazole-4-carboxylic acid
CAS NO:108403-90-3
Molecular Formula:
Molecular Weight: 389.819
EINECS: N/A
Product Categories: N/A
Mol File: 108403-90-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-Benzyl-2-(4-chloro-2-nitro-phenylsulfanyl)-3H-imidazole-4-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: 3-Benzyl-2-(4-chloro-2-nitro-phenylsulfanyl)-3H-imidazole-4-carboxylic acid(108403-90-3)
EPA Substance Registry System: 3-Benzyl-2-(4-chloro-2-nitro-phenylsulfanyl)-3H-imidazole-4-carboxylic acid(108403-90-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 108403-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 108403-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,0 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 108403-90:
(8*1)+(7*0)+(6*8)+(5*4)+(4*0)+(3*3)+(2*9)+(1*0)=103
103 % 10 = 3
So 108403-90-3 is a valid CAS Registry Number.

108403-90-3Upstream product

108403-90-3Downstream Products

108403-95-8 3-Benzyl-2-(4-chloro-2-nitro-phenylsulfanyl)-3H-imidazole-4-carbonyl chloride

108403-90-3Relevant articles and documents

New imidazole-5-carbohydroxamic acids with biological activity

Bossio,Capei,Marcaccini,Pepino,Tiscione

, p. 377 - 379 (2007/10/02)

A series of 1-benzyl-2-arylthio (or heteroarylthio)-5-imidazolecarbohydroxamic acids (Va-e) was prepared starting from the corresponding imidazole-5-carboxylic acids IIIa-e via acid chlorides IVa-e. Tests of biological activity showed that compounds Va-e are fairly active against Escherichia coli and Candida albicans.

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