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234082-35-0

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234082-35-0 Usage

Chemical Properties

off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 234082-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,4,0,8 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 234082-35:
(8*2)+(7*3)+(6*4)+(5*0)+(4*8)+(3*2)+(2*3)+(1*5)=110
110 % 10 = 0
So 234082-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClFO2/c1-12-8(11)5-2-3-7(10)6(9)4-5/h2-4H,1H3

234082-35-0SDS

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 Methyl 3-chloro-4-fluorobenzoate

1.2 Other means of identification

Product number -
Other names 3-Chloro-4-fluoro-benzoic acid methyl ester

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:234082-35-0 SDS

234082-35-0Relevant articles and documents

POLY-ADP RIBOSE POLYMERASE (PARP) INHIBITORS

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Page/Page column 30, (2018/07/29)

The present invention is related to a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and a compound represented by the following structural formula: The present invention is also related a method of treating a subject with a disease which can be ameliorated by inhibition of poly(ADP-ribose)polymerase (PARP). The definitions of the variables are provided herein.

Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides

Rando, Daniela G.,Avery, Mitchell A.,Tekwani, Babu L.,Khan, Shabana I.,Ferreira, Elizabeth I.

, p. 6724 - 6731 (2008/12/22)

A series of 53 nitro derivatives rationally designed were obtained by parallel synthesis and screened against Leishmania donovani. Six compounds exhibited IC50 values lower than standard drugs. Brief SAR analysis revealed that substitution is important to the activity. Nitrothiophene analogues were more potent than the nitrofuran ones. This was attributed to the ability of sulfur atoms in accommodating electrons from nitro group, which facilitate its reduction and therefore the formation of free radicals lethal to parasites.

PROCESS FOR THE MANUFACTURE OF 4-FLUORO-ANTHRANILIC ACID

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Page/Page column 6, (2008/06/13)

The present invention concerns a process for preparing 4-fluoro-anthranilic acid by nitration, reduction and hydrolysis of an alkyl 3-chloro-4-fluorobenzoate.

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