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118745-63-4

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118745-63-4 Usage

Uses

2-Fluoro-4-methylbenzyl bromide is used as a pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 118745-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118745-63:
(8*1)+(7*1)+(6*8)+(5*7)+(4*4)+(3*5)+(2*6)+(1*3)=144
144 % 10 = 4
So 118745-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrF/c1-6-2-3-7(5-9)8(10)4-6/h2-4H,5H2,1H3

118745-63-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H26440)  2-Fluoro-4-methylbenzyl bromide, 97%   

  • 118745-63-4

  • 1g

  • 2161.0CNY

  • Detail
  • Alfa Aesar

  • (H26440)  2-Fluoro-4-methylbenzyl bromide, 97%   

  • 118745-63-4

  • 5g

  • 6637.0CNY

  • Detail

118745-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(bromomethyl)-2-fluoro-4-methylbenzene

1.2 Other means of identification

Product number -
Other names JRD-1374

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:118745-63-4 SDS

118745-63-4Upstream product

118745-63-4Downstream Products

118745-63-4Relevant articles and documents

SYNTHESIS AND STEREOISOMER SEPARATION OF DIFLUOROPARACYCLOPHANE

Huang, Xiaadling,Qu, Fanqi,Li, Zadying

, p. 33 - 40 (2007/10/02)

Difluoroparacyclophane was synthesized by 1,6-Hofmann elimaination of 2-fluoro-4-methylbenzyltrimethyl ammonium hydroxide in 34percent yield and four stereoisomer were separated by TLC and HPLC techniques.

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