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71274-84-5

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71274-84-5 Usage

General Description

4-Trifluoromethoxy-biphenyl, also known as 4-(Trifluoromethoxy)biphenyl or TFMOP, is a chemical compound consisting of a biphenyl molecule with a trifluoromethoxy group attached. It is a colorless to light yellow liquid with a molecular weight of 234.1 g/mol. 4-Trifluoromethoxy-biphenyl is used as a building block in the synthesis of various organic compounds and pharmaceuticals. It is also used as a reagent in organic chemistry reactions, particularly in the preparation of biologically active molecules. The trifluoromethoxy group in the compound imparts unique chemical and physical properties, making it a valuable tool in chemical and pharmaceutical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 71274-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,7 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71274-84:
(7*7)+(6*1)+(5*2)+(4*7)+(3*4)+(2*8)+(1*4)=125
125 % 10 = 5
So 71274-84-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H9F3O/c14-13(15,16)17-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H

71274-84-5SDS

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 1-phenyl-4-(trifluoromethoxy)benzene

1.2 Other means of identification

Product number -
Other names 4-Phenylphenyl trifluoromethyl ether

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:71274-84-5 SDS

71274-84-5Relevant articles and documents

Phenyl hydrazine as initiator for direct arene C-H arylation via base promoted homolytic aromatic substitution

Dewanji, Abhishek,Murarka, Sandip,Curran, Dennis P.,Studer, Armido

supporting information, p. 6102 - 6105 (2014/01/06)

A simple and efficient direct radical arylation of unactivated arenes is described which uses cheap and commercially available phenyl hydrazine as an initiator. The reaction occurs through a base promoted homolytic aromatic substitution (BHAS) mechanism involving aryl radicals and aryl radical anions as intermediates and offers a practical approach for preparation of an array of substituted biaryls.

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