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202001-00-1

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202001-00-1 Usage

Chemical Properties

White crystalline powder and chunks

Check Digit Verification of cas no

The CAS Registry Mumber 202001-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,0,0 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 202001-00:
(8*2)+(7*0)+(6*2)+(5*0)+(4*0)+(3*1)+(2*0)+(1*0)=31
31 % 10 = 1
So 202001-00-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClFO2/c9-6-1-5(3-8(11)12)2-7(10)4-6/h1-2,4H,3H2,(H,11,12)

202001-00-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H26665)  3-Chloro-5-fluorophenylacetic acid, 97%   

  • 202001-00-1

  • 250mg

  • 653.0CNY

  • Detail
  • Alfa Aesar

  • (H26665)  3-Chloro-5-fluorophenylacetic acid, 97%   

  • 202001-00-1

  • 1g

  • 2007.0CNY

  • Detail

202001-00-1SDS

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 2-(3-chloro-5-fluorophenyl)acetic acid

1.2 Other means of identification

Product number -
Other names (3-CHLORO-5-FLUOROPHENYL)ACETIC ACID

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:202001-00-1 SDS

202001-00-1Relevant articles and documents

Synthesis of dihalophenylacetic acids using aromatic nucleophilic substitution strategy

Kowalczyk, Bruce A.

, p. 1411 - 1414 (2007/10/03)

A simple synthetic strategy to dihalophenylacetic acids and specifically 3,5-difluorophenylacetic acid an important pharmaceutical intermediate was developed. The aromatic nucleophilic substitution of dihalofluorobenzenes using the anion of ethyl cyanoacetate yielded ethyl dihalophenylcyanoacetates. The basic decarboxylation of the ethyl dihalophenylcyanoacetates produced targeted dihalophenylacetic acids.

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