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2-(4-FLUOROPHENYL)-5-METHOXY-1H-BENZO[D]IMIDAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20100-21-4

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20100-21-4 Usage

General Description

2-(4-Fluorophenyl)-5-methoxy-1H-benzo[d]imidazole is a chemical compound with the molecular formula C14H11FN2O. It is a heterocyclic compound that contains a benzimidazole ring system, with a fluorophenyl group and a methoxy group attached to it. 2-(4-FLUOROPHENYL)-5-METHOXY-1H-BENZO[D]IMIDAZOLE is known for its potential pharmacological activities and is of interest in medicinal chemistry research for its potential use in drug development. It may exhibit various biological activities and can be used as a building block in the synthesis of novel pharmaceutical compounds. Further research is ongoing to explore its potential applications in medicine and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 20100-21-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,0 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20100-21:
(7*2)+(6*0)+(5*1)+(4*0)+(3*0)+(2*2)+(1*1)=24
24 % 10 = 4
So 20100-21-4 is a valid CAS Registry Number.

20100-21-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-fluorophenyl)-6-methoxy-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names -

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:20100-21-4 SDS

20100-21-4Downstream Products

20100-21-4Relevant academic research and scientific papers

A novel synthesis of 2-arylbenzimidazoles in molecular sieves-MeOH system and their antitubercular activity

Chaturvedi, Amit K.,Verma, Amit Kumar,Thakur, Jay Prakash,Roy, Sudeep,Bhushan Tripathi, Shashi,Kumar, Balagani Sathish,Khwaja, Sadiya,Sachan, Naresh K.,Sharma, Ashok,Chanda, Debabrata,Shanker, Karuna,Saikia, Dharmendra,Negi, Arvind S.

, p. 4551 - 4559 (2018/08/11)

Arylbenzimidazoles have been synthesized as antimycobacterial agents. An efficient synthesis has been developed for 2-arylbenzimidazoles from o-phenylenediamines and aromatic aldehydes in molecular sieves-methanol system. The methodology is straightforward to get 2-arylbenzimidazoles (3a–3z) in excellent yields with high chemoselectivity over 2-aryl-1-benzylbenzimidazoles (4a–4z). All these benzimidazole analogues were evaluated against M. tuberculosis in BACTEC radiometric assay. The compounds 4y and 4z exhibited potential antitubercular activity against M. tuberculosis H37RV, MIC at 16 μM and 24 μM respectively. The best compound of the series i.e. compound 4y was well tolerated by Swiss-albino mice in acute oral toxicity. Compound 4y possessing a diarylbenzimidazole core, can further be optimized for better activity.

A simple and straightforward synthesis of substituted 2-arylbenzimidazoles over silica gel

Chaturvedi, Amit K.,Negi, Arvind S.,Khare, Puja

, p. 4500 - 4504 (2013/04/24)

A solid phase strategy for the synthesis of substituted 2-arylbenzimidazoles over silica gel has been achieved starting from their corresponding o-phenylenediamines 1 and aromatic aldehydes 2. The reaction is very simple, convenient and straightforward, a

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