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Benzoic acid, 4-(5-chloro-1H-benzimidazol-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

204514-08-9

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204514-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204514-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,5,1 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 204514-08:
(8*2)+(7*0)+(6*4)+(5*5)+(4*1)+(3*4)+(2*0)+(1*8)=89
89 % 10 = 9
So 204514-08-9 is a valid CAS Registry Number.

204514-08-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(6-chloro-1H-benzimidazol-2-yl)benzoic acid

1.2 Other means of identification

Product number -
Other names 4-(5-chloro-1H-benzoimidazol-2-yl)-benzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:204514-08-9 SDS

204514-08-9Relevant academic research and scientific papers

Single bead IR monitoring of a novel benzimidazole synthesis

Sun, Qun,Yan, Bing

, p. 361 - 364 (1998)

A novel and efficient solid-phase synthesis of benzimidazoles and the monitoring of all conversions in this synthesis are reported.

Synthesis and antimicrobial activity of some novel 2-[4-(substituted piperazin-/piperidin-1-ylcarbonyl)phenyl]- 1 H-benzimidazole derivatives

Kus, Canan,Soezuedoenmez, Fatma,Altanlar, Nurten

experimental part, p. 54 - 60 (2009/06/18)

In this study, we report the synthesis and antimicrobial evaluation of several new 4-(1H-benzimi-dazol-2-yl)benzamides (11 - 30) and 5-chloro-1-(p-fluorobenzyl)-2-{4-[(4-methylpiperazin-1-yl)carbonyl]phenyl} -1H-benzimidazole (33). Compound 20 exhibited the best antibacterial activity with MIC value of 6.25 μg/mL against Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA). Significant antifungal activities were obtained with the compounds 13, 14, 18, 19, and 33 with MIC values of 3.12 μg/mL which are close to fluconazole.

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