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326-64-7

326-64-7

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326-64-7 Usage

Uses

5-Chloro-2-(trifluoromethoxy)aniline

Check Digit Verification of cas no

The CAS Registry Mumber 326-64-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 326-64:
(5*3)+(4*2)+(3*6)+(2*6)+(1*4)=57
57 % 10 = 7
So 326-64-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClF3NO/c8-4-1-2-6(5(12)3-4)13-7(9,10)11/h1-3H,12H2

326-64-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H32259)  5-Chloro-2-(trifluoromethoxy)aniline, 97%   

  • 326-64-7

  • 250mg

  • 480.0CNY

  • Detail

  • Alfa Aesar

  • (H32259)  5-Chloro-2-(trifluoromethoxy)aniline, 97%   

  • 326-64-7

  • 1g

  • 1605.0CNY

  • Detail

326-64-7SDS

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 5-chloro-2-(trifluoromethoxy)aniline

1.2 Other means of identification

Product number -
Other names 5-Chloro-2-trifluoro Methoxy aniline

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:326-64-7 SDS

326-64-7Relevant articles and documents

Method for preparing 2-trifluoro-methoxy-aniline

-

, (2008/06/13)

PCT No. PCT/FR98/01050 Sec. 371 Date Nov. 29, 1999 Sec. 102(e) Date Nov. 29, 1999 PCT Filed May 26, 1998 PCT Pub. No. WO98/54121 PCT Pub. Date Dec. 3, 1998This invention relates to a method for the preparation of a compound of formula I comprising the steps consisting in: a) optionally reacting a compound of general formula II: with a nitration reagent b) reducing the compound obtained in a) c) subjecting the compound obtained in b) to a dehydrochlorination in order to obtain the compound of formula I: and d) isolating the compound obtained in step c) from the reaction mixture.

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