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207226-31-1

207226-31-1

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207226-31-1 Usage

Uses

1,3-Dibromo-5-(trifluoromethoxy)benzene may be used in chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 207226-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,2,2 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 207226-31:
(8*2)+(7*0)+(6*7)+(5*2)+(4*2)+(3*6)+(2*3)+(1*1)=101
101 % 10 = 1
So 207226-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Br2F3O/c8-4-1-5(9)3-6(2-4)13-7(10,11)12/h1-3H

207226-31-1 Well-known Company Product Price

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  • TCI America

  • (D3322)  1,3-Dibromo-5-(trifluoromethoxy)benzene  >98.0%(GC)

  • 207226-31-1

  • 5g

  • 620.00CNY

  • Detail

  • TCI America

  • (D3322)  1,3-Dibromo-5-(trifluoromethoxy)benzene  >98.0%(GC)

  • 207226-31-1

  • 25g

  • 2,150.00CNY

  • Detail

  • Alfa Aesar

  • (H64115)  1,3-Dibromo-5-(trifluoromethoxy)benzene, 97%   

  • 207226-31-1

  • 5g

  • 196.0CNY

  • Detail

  • Alfa Aesar

  • (H64115)  1,3-Dibromo-5-(trifluoromethoxy)benzene, 97%   

  • 207226-31-1

  • 25g

  • 588.0CNY

  • Detail

  • Alfa Aesar

  • (H64115)  1,3-Dibromo-5-(trifluoromethoxy)benzene, 97%   

  • 207226-31-1

  • 100g

  • 1862.0CNY

  • Detail

207226-31-1SDS

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 1,3-DIBROMO-5-(TRIFLUOROMETHOXY)BENZENE

1.2 Other means of identification

Product number -
Other names 1,3-Dibromo-5-trifluoromethoxy-benzene

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:207226-31-1 SDS

207226-31-1Relevant articles and documents

Silver-Mediated Trifluoromethoxylation of (Hetero)aryldiazonium Tetrafluoroborates

Yang, Yu-Ming,Yao, Jian-Fei,Yan, Wei,Luo, Zhuangzhu,Tang, Zhen-Yu

supporting information, p. 8003 - 8007 (2019/10/11)

Here we report a silver-mediated trifluoromethoxylation of (hetero)aryldiazonium tetrafluoroborates by converting an aromatic amino group into an OCF3 group. This method, which can be considered to be a trifluoromethoxylation variation of the classic Sandmeyer-type reaction, uses readily available aryl and heteroaromatic amines as starting materials and AgOCF3 as trifluoromethoxylating reagents. The broad substrate scope and simple, mild reaction condition made this transformation a valuable method in constructing aryl-OCF3 bonds.

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