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403-61-2

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403-61-2 Usage

General Description

The chemical 4-(2-chloro-1,1,2-trifluoro-ethoxy)-phenylamine is an organic compound that contains a phenylamine group attached to a 2-chloro-1,1,2-trifluoroethoxy group. It is commonly used as an intermediate or building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. The presence of the chloro and trifluoro groups in this chemical makes it a valuable reagent for the synthesis of complex organic molecules. Additionally, these functional groups can impart specific properties to the resulting compounds, making 4-(2-chloro-1,1,2-trifluoro-ethoxy)-phenylamine an important component in the development of new materials and substances.

Check Digit Verification of cas no

The CAS Registry Mumber 403-61-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 403-61:
(5*4)+(4*0)+(3*3)+(2*6)+(1*1)=42
42 % 10 = 2
So 403-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClF3NO/c9-7(10)8(11,12)14-6-3-1-5(13)2-4-6/h1-4,7H,13H2

403-61-2SDS

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 4-(2-chloro-1,1,2-trifluoroethoxy)aniline

1.2 Other means of identification

Product number -
Other names 4-(1,1,2-trifluoro-2-chloroethoxy)aniline

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:403-61-2 SDS

403-61-2Relevant articles and documents

Phenols reactions with 1,1-difluorodichloroethene, 1,2-di(fluorochloro) ethene, and trifluorochloroethene

Kremlev,Mushta,Moklyarchuk

, p. 1125 - 1129 (2007/10/03)

Phenols containing in the para-position of the benzene ring substituents of various electronic character add to 1,1-difluorodichloroethene in acetone in the presence of potassium hydroxide. A similar reaction with 1,2-di(fluorochloro)ethene occurs only in

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