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202859-73-2

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  • SAGECHEM/1-cyclopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one/SAGECHEM/Manufacturer in China

    Cas No: 202859-73-2

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202859-73-2 Usage

General Description

1-Cyclopropyl-1,3-dihydro-2H-benzimidazol-2-one is a chemical compound that belongs to the class of benzimidazolones. It is a cyclic compound with a cyclopropyl group attached to the benzimidazole ring. 1-Cyclopropyl-1,3-dihydro-2H-benzimidazol-2-one has potential pharmacological activities, and is being studied for its potential therapeutic applications. It may have potential use in the treatment of various diseases and conditions, and its chemical structure makes it a valuable target for medicinal chemistry research. Further studies are warranted to fully understand the properties and potential applications of 1-Cyclopropyl-1,3-dihydro-2H-benzimidazol-2-one.

Check Digit Verification of cas no

The CAS Registry Mumber 202859-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,8,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 202859-73:
(8*2)+(7*0)+(6*2)+(5*8)+(4*5)+(3*9)+(2*7)+(1*3)=132
132 % 10 = 2
So 202859-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O/c13-10-11-8-3-1-2-4-9(8)12(10)7-5-6-7/h1-4,7H,5-6H2,(H,11,13)

202859-73-2SDS

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 3-cyclopropyl-1H-benzimidazol-2-one

1.2 Other means of identification

Product number -
Other names 1-cyclopropyl-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:202859-73-2 SDS

202859-73-2Relevant articles and documents

PYRIMIDINE OR PYRIDINE COMPOUNDS, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL USES THEREOF

-

, (2017/09/19)

The present invention disclosed a class of pyrimidine or pyridine compounds, pharmaceutically acceptable salts, stereoisomers, prodrugs and solvates thereof, preparation method therefor and pharmaceutical compositions and pharmaceutical uses thereof. The compounds can inhibit the variants of EGFR (Epidermis Growth Factor Receptor) proteinases, and therefore can inhibit the growth of a variety of tumor cells effectively. The compounds can be used to prepare antitumor drugs, used for the treatment, combined therapy or prevention of various different cancers. The compounds can overcome the drug resistance induced by the existing first-generation EGFR inhibitors such as gefitinib, erlotinib and so on. Particularly, the compounds can be used to prepare drugs for treating or preventing diseases, disturbances, disorders or conditions mediated by epidermis growth factor receptor variants (such as L858R activated mutants, Exon19 deletion activated mutants and T790M resistant mutants).

RESPIRATORY SYNCYTIAL VIRUS INHIBITORS

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, (2015/05/19)

Compounds of Formula (I): wherein R1, R2 and R3 are defined herein, are useful as inhibitors of RSV.

Synthesis and activity of novel 1- or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors

Zhang, Puwen,Terefenko, Eugene A.,McComas, Casey C.,Mahaney, Paige E.,Vu, An,Trybulski, Eugene,Koury, Elizabeth,Johnston, Grace,Bray, Jenifer,Deecher, Darlene

scheme or table, p. 6067 - 6070 (2009/08/07)

A series of novel 1- or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors was discovered. Several compounds such as 15 and 20 showed good hNET potency. Compounds 15 and 20 also displayed excellent selectivity at hNET that appeared superior to those of reboxetine and atomoxetine (4 and 5).

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