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BENZIMIDAZOLE, 4-METHOXY-2-METHYL- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27077-75-4

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27077-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27077-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,7 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27077-75:
(7*2)+(6*7)+(5*0)+(4*7)+(3*7)+(2*7)+(1*5)=124
124 % 10 = 4
So 27077-75-4 is a valid CAS Registry Number.

27077-75-4SDS

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 4-methoxy-2-methyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 4-methoxy-2-methyl-1H-benzo[d]imidazole

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:27077-75-4 SDS

27077-75-4Relevant academic research and scientific papers

BICYCLIC HETEROARYL DERIVATIVES AS ECTONUCLEOTIDE PYROPHOSPHATASE PHOSPHODIESTERASE 1 INHIBITORS

-

Paragraph 0347; 0396, (2020/10/21)

The present disclosure provides certain bicyclic heteroaryl compounds that inhibit ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) enzymatic activity and are therefore useful for the treatment of diseases and conditions modulated at least in part by ENPP1. In some embodiments, the bicyclic heteroaryl compounds includes those of Formula (I). Also provided herein are pharmaceutical compositions containing such compounds and processes for preparing such compounds.

Novel strategy for synthesis of substituted benzimidazo[1,2-a]quinolines

Kato, Jun-Ya,Ito, Yutaro,Ijuin, Ryosuke,Aoyama, Hiroshi,Yokomatsu, Tsutomu

supporting information, p. 3794 - 3797 (2013/08/23)

An efficient method for the synthesis of benzimidazo[1,2-a]quinolines under transition-metal-free conditions has been developed through a cascade reaction involving sequential aromatic nucleophilic substitution and intramolecular Knoevenagel condensation reactions. This method is applicable for the synthesis of a wide range of benzimidazo[1,2-a]quinoline derivatives from readily available 2-fluoroarylaldehyde and benzimidazole substrates.

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