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5-Methoxy-1,3-dimethyl-1H-benzo[d]imidazol-2(3H)-one is a chemical compound with the molecular formula C10H11N2O2. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. The compound features a methoxy group (-OCH3) at the 5-position, and two methyl groups (-CH3) at the 1 and 3 positions. The 2(3H)-one functional group indicates the presence of a ketone group at the 2-position. 5-Methoxy-1,3-diMethyl-1H-benzo[d]iMidazol-2(3H)-one is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block for the synthesis of various bioactive molecules. Its structure and properties make it a versatile intermediate in organic synthesis, with potential uses in the development of new drugs and chemical compounds.

64107-38-6

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64107-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64107-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,0 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64107-38:
(7*6)+(6*4)+(5*1)+(4*0)+(3*7)+(2*3)+(1*8)=106
106 % 10 = 6
So 64107-38-6 is a valid CAS Registry Number.

64107-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-1,3-dimethyl-1H-benzo[d]imidazol-2(3H)-one

1.2 Other means of identification

Product number -
Other names 5-Methoxy-1,3-dimethyl-1,3-dihydro-benzoimidazol-2-one

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:64107-38-6 SDS

64107-38-6Relevant academic research and scientific papers

GSK6853, a Chemical Probe for Inhibition of the BRPF1 Bromodomain

Bamborough, Paul,Barnett, Heather A.,Becher, Isabelle,Bird, Mark J.,Chung, Chun-Wa,Craggs, Peter D.,Demont, Emmanuel H.,Diallo, Hawa,Fallon, David J.,Gordon, Laurie J.,Grandi, Paola,Hobbs, Clare I.,Hooper-Greenhill, Edward,Jones, Emma J.,Law, Robert P.,Le Gall, Armelle,Lugo, David,Michon, Anne-Marie,Mitchell, Darren J.,Prinjha, Rab K.,Sheppard, Robert J.,Watson, Allan J. B.,Watson, Robert J.

supporting information, p. 552 - 557 (2016/07/06)

The BRPF (Bromodomain and PHD Finger-containing) protein family are important scaffolding proteins for assembly of MYST histone acetyltransferase complexes. A selective benzimidazolone BRPF1 inhibitor showing micromolar activity in a cellular target engag

Copper-catalyzed efficient synthesis of a 2-benzimidazolone scaffold from 2-nitroaniline and dimethyl carbonate via a hydrosilylation reaction

Nale, Deepak B.,Bhanage, Bhalchandra M.

, p. 2480 - 2486 (2015/04/27)

This work reports a copper-catalyzed novel protocol for the tandem synthesis of 2-benzimidazolone derivatives from dimethyl carbonate (DMC) and various 2-nitroanilines by using polymethylhydrosiloxane (PMHS) as an inexpensive, stable and environmentally benign reducing agent. This methodology is applicable for the preparation of a broad range of biologically active 2-benzimidazolone derivatives with a good scope in good to excellent yields.

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