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BENZENE, 1,2-DICHLORO-3-NITRO-4-(TRIFLUOROMETHYL)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133391-72-7

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133391-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133391-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,9 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133391-72:
(8*1)+(7*3)+(6*3)+(5*3)+(4*9)+(3*1)+(2*7)+(1*2)=117
117 % 10 = 7
So 133391-72-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H2Cl2F3NO2/c8-4-2-1-3(7(10,11)12)6(5(4)9)13(14)15/h1-2H

133391-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Dichloro-3-nitro-4-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 2-Trifluoromethyl-5,6-dichloronitrobenzene

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:133391-72-7 SDS

133391-72-7Downstream Products

133391-72-7Relevant academic research and scientific papers

THE TRIFLUOROMETHYLATION OF CHLOROAROMATICS USING THE COPPER-CF2Br2-DIALKYLAMIDE REACTION SYSTEM

Clark, James H.,Denness, James E.,McClinton, Martin A.,Wynd, Andrew J.

, p. 411 - 426 (2007/10/02)

The in situ generation of CuCF3 from the reaction of copper, dibromodifluoromethane and either N,N-dimethylformamide or N,N-dimethylacetamide (Burton's reagent) has been used for the direct substitution of chlorine by CF3 in a number of aromatic substrates.Particular attention has been paid to the effects of ring substituents on the efficiency of reaction.

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