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118794-10-8

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118794-10-8 Usage

General Description

5-CHLORO-6-METHYLBENZO[D]OXAZOL-2(3H)-ONE is a chemical compound with the molecular formula C8H5ClNO2. It is a heterocyclic compound containing a benzoxazole ring with a chlorine atom at the 5-position and a methyl group at the 6-position. 5-CHLORO-6-METHYLBENZO[D]OXAZOL-2(3H)-ONE is commonly used in organic synthesis as a starting material for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. It has also been studied for its potential pharmacological activities, including its antimicrobial, antiviral, and antitumor properties. Additionally, 5-CHLORO-6-METHYLBENZO[D]OXAZOL-2(3H)-ONE has been used as a building block in the development of new materials and as a precursor for the synthesis of novel chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 118794-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,9 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 118794-10:
(8*1)+(7*1)+(6*8)+(5*7)+(4*9)+(3*4)+(2*1)+(1*0)=148
148 % 10 = 8
So 118794-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClNO2/c1-4-2-7-6(3-5(4)9)10-8(11)12-7/h2-3H,1H3,(H,10,11)

118794-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-6-methyl-3H-1,3-benzoxazol-2-one

1.2 Other means of identification

Product number -
Other names 5-chloro-6-methylbenzoxazolin-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:118794-10-8 SDS

118794-10-8Relevant articles and documents

The discovery of potent and selective kynurenine 3-monooxygenase inhibitors for the treatment of acute pancreatitis

Liddle, John,Beaufils, Benjamin,Binnie, Margaret,Bouillot, Anne,Denis, Alexis A.,Hann, Michael M.,Haslam, Carl P.,Holmes, Duncan S.,Hutchinson, Jon P.,Kranz, Michael,McBride, Andrew,Mirguet, Olivier,Mole, Damian J.,Mowat, Christopher G.,Pal, Sandeep,Rowland, Paul,Trottet, Lionel,Uings, Iain J.,Walker, Ann L.,Webster, Scott P.

, p. 2023 - 2028 (2017)

A series of potent, competitive and highly selective kynurenine monooxygenase inhibitors have been discovered via a substrate-based approach for the treatment of acute pancreatitis. The lead compound demonstrated good cellular potency and clear pharmacodynamic activity in vivo.

3-(5-CHLORO-2-OXOBENZO[D]OXAZOL-3(2H)-YL)PROPANOIC ACID DERIVATIVES AS KMO INHIBITORS

-

, (2015/07/07)

A compound of formula (I) or a salt thereof are provided wherein R1, X and R3 are defined in the specification, useful in the treatment of disorders mediated by KMO such as acute pancreatitis, chronic kidney disease, other conditions associated with systemic inflammatory response syndrome (SIRS), Huntington's disease, Alzheimer's disease, spinocerebellar ataxias, Parkinson's disease, AIDS-dementia complex, amylotrophic lateral sclerosis (ALS), depression, schizophrenia, sepsis, cardiovascular shock, severe trauma, acute lung injury, acute respiratory distress syndrome, acute cholecystitis, severe burns, pneumonia, extensive surgical procedures, ischemic bowel, severe acute hepatic disease, severe acute hepatic encephalopathy or acute renal failure.

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