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32137-20-5

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32137-20-5 Usage

General Description

4-CHLORO-3-FLUOROBENZOTRIFLUORIDE is an organic compound with the chemical formula C7H3ClF4. It is a colorless liquid that is insoluble in water but soluble in organic solvents. The compound is used as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a reagent in the synthesis of various organic compounds. 4-CHLORO-3-FLUOROBENZOTRIFLUORIDE is known for its high thermal stability and chemical inertness, making it a valuable building block in the chemical industry. However, it is important to handle this compound with care as it may be harmful if ingested, inhaled, or absorbed through the skin, and it can cause irritation to the eyes and skin.

Check Digit Verification of cas no

The CAS Registry Mumber 32137-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,3 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32137-20:
(7*3)+(6*2)+(5*1)+(4*3)+(3*7)+(2*2)+(1*0)=75
75 % 10 = 5
So 32137-20-5 is a valid CAS Registry Number.

32137-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-3-fluorobenzotrifluoride

1.2 Other means of identification

Product number -
Other names 1-Chloro-2-fluoro-4-(trifluoromethyl)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:32137-20-5 SDS

32137-20-5Relevant articles and documents

Large-scale preparation of aromatic fluorides via electrophilic fluorination with functionalized aryl- or heteroarylmagnesium reagents

Yamada, Shigeyuki,Knochel, Paul

experimental part, p. 2490 - 2494 (2010/09/04)

Functionalized aryl- or heteroarylmagnesium reagents, prepared from the corresponding bromides or iodides using halogen-magnesium exchange or direct magnesium insertion in the presence of lithium chloride, reacted smoothly with N-fluorobenzenesulfonimide, (PhSO2)2NF, in the mixed solvent (4:1 CH2Cl2-perfluorodecalin) to give the corresponding aromatic fluorides in moderate to good yields. Georg Thieme Verlag Stuttgart · New York.

AROMATIC FLUORINE CHEMISTRY. PART 1. 3,4-DIFLUOROBENZOIC ACID AND DERIVATIVES VIA 3,4-DIFLUOROBENZOTRIFLUORIDE

Pews, R. G.,Gall, J. A.,Little, J. C.

, p. 365 - 370 (2007/10/02)

The preparation of 3,4-difluorobenzotrifluoride from 3,4-dichlorobenzotrifluoride by a KF exchange reaction is described.The conversion of 3,4-difluorobenzotrifluoride to 3,4-difluorobenzoic acid and derivatives is also reported.

THE FLUORINATION OF ORGANIC SUBSTRATES WITH TETRAPHENYLPHOSPHONIUM HYDROGENDIFLUORIDE

Brown, S. J.,Clark, J. H.

, p. 251 - 258 (2007/10/02)

Tetraphenylphosphonium hydrogendifluoride acts as a powerful source of F- in various reactions with organic substrates to give fluorine containing products.

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