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243139-71-1

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243139-71-1 Usage

Uses

2,4,5-Trifluorobenzyl chloride is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 243139-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,1,3 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 243139-71:
(8*2)+(7*4)+(6*3)+(5*1)+(4*3)+(3*9)+(2*7)+(1*1)=121
121 % 10 = 1
So 243139-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6F4O2/c1-14-8-6(11)4(9)3(2-13)5(10)7(8)12/h13H,2H2,1H3

243139-71-1 Well-known Company Product Price

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  • Alfa Aesar

  • (B20470)  2,4,5-Trifluorobenzyl chloride, 97%   

  • 243139-71-1

  • 1g

  • 607.0CNY

  • Detail
  • Alfa Aesar

  • (B20470)  2,4,5-Trifluorobenzyl chloride, 97%   

  • 243139-71-1

  • 5g

  • 2427.0CNY

  • Detail

243139-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(chloromethyl)-2,4,5-trifluorobenzene

1.2 Other means of identification

Product number -
Other names 2,4,5-TRIFLUOROBENZYL CHLORIDE

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:243139-71-1 SDS

243139-71-1Relevant articles and documents

Preparation method of 2,4,5-trifluorophenylacetic acid

-

, (2021/05/29)

The invention belongs to the technical field of preparation of drug intermediates, and discloses a preparation method of 2,4,5-trifluorophenylacetic acid, wherein the preparation method comprises the steps: step 1, reacting raw materials, a quaternary ammonium salt catalyst, sulfolane and potassium fluoride to obtain a first intermediate; step 2, carrying out hydrogenation catalytic reaction on the first intermediate to obtain a second intermediate; step 3, carrying out salt forming reaction on the second intermediate and a fluorinating reagent, quenching, and carrying out diazotization reaction on the second intermediate and a sodium nitrite aqueous solution to obtain diazonium salt; step 4, carrying out high-temperature cracking on the diazonium salt, to obtain 2,4,5-trifluorotoluene; and step 5 to step 7, carrying out halogenation, cyanidation and hydrolysis reactions on 2,4,5-trifluorotoluene in sequence, and thus obtaining 2,4,5-trifluorophenylacetic acid. The raw materials adopted by the method are easy to obtain and low in cost, the yield of the corresponding product obtained in each step is high, and large-scale production of the 2,4,5-trifluorophenylacetic acid is facilitated.

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