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Benzenamine, 4-[(trifluoromethyl)sulfinyl]-, also known as 4-(trifluoromethyl)sulfinylaniline or 4-(trifluoromethylsulfanyl)aniline, is an organic compound with the chemical formula C7H7F3NS. It is a derivative of aniline, where a trifluoromethylsulfinyl group replaces one of the hydrogen atoms on the benzene ring. Benzenamine, 4-[(trifluoromethyl)sulfinyl]- is characterized by its unique chemical structure, which features a sulfur atom bonded to a trifluoromethyl group and an amino group. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry and chemical engineering.

708-67-8

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708-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 708-67-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 708-67:
(5*7)+(4*0)+(3*8)+(2*6)+(1*7)=78
78 % 10 = 8
So 708-67-8 is a valid CAS Registry Number.

708-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(trifluoromethylsulfinyl)aniline

1.2 Other means of identification

Product number -
Other names (4-Acetamino-phenyl)-trifluormethyl-sulfoxid

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:708-67-8 SDS

708-67-8Relevant academic research and scientific papers

Selective oxidation and chlorination of trifluoromethylsulfide using trichloroisocyanuric acid in ionic liquid

Tang, Ri-Yuan,Zhong, Ping,Lin, Qiu-Lian

, p. 636 - 640 (2008/01/06)

A route to chemoselective oxidation and chlorination of aryltrifluoromethylsulfide using trichloroisocyanuric acid (TCCA) in ionic liquid, an efficiently O-methylation reaction and a reduction of nitro- to amido- in excellent yields have been developed.

Aryltrifluoromethylsulfoxides: Sulfinylation of aromatics by triflinate salts in acid medium

Wakselman,Tordeux,Freslon,Saint-Jalmes

, p. 550 - 552 (2007/10/03)

Direct sulfinylation reaction of simple aromatic compounds by triflinate salts in triflic acid led to aryltrifluoromethyl sulfoxides. The para isomer was the major one. The regioselectivity of the reaction was very high when the substituent on the aromatic ring was a halogen atom, a trifluoromethoxy group or an acetanilide function.

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