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3,4,5-trichloro-2,6-difluoronitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136272-32-7

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136272-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136272-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,7 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136272-32:
(8*1)+(7*3)+(6*6)+(5*2)+(4*7)+(3*2)+(2*3)+(1*2)=117
117 % 10 = 7
So 136272-32-7 is a valid CAS Registry Number.

136272-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5-trichloro-2,6-difluoronitrobenzene

1.2 Other means of identification

Product number -
Other names 2,6-difluoro-3,4,5-trichloronitrobenzene

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:136272-32-7 SDS

136272-32-7Relevant academic research and scientific papers

AROMATIC FLUORINE CHEMISTRY. PART 4. PREPARATION OF 2,6-DIFLUOROANILINE

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

, p. 307 - 316 (2007/10/02)

The preparation of 2,6-difluoroaniline from 1,3,5-trichlorobenzene is described. 1-Chloro-3,5-difluorobenzene prepared via KF exchange on 1,3,5-trichlorobenzene is dichlorinated and nitrated in a single reactor to a mixture of trichlorodifluoronitrobenzenes.The latter are reduced to ca. 4:1 mixture of 2,6-difluoroaniline and 2,4-difluoroaniline.

Process and intermediates for the preparation of 2,6-difluoroaniline

-

, (2008/06/13)

1-Chloro-3,5-difluorobenzene is chlorinated to give 4,6-difluoro-1,2,3-trichlorobenzene which in turn is nitrated and reduced to the corresponding novel aniline, 2,6-difluoro-3,4,5-trichloroaniline. Further reduction of this aniline provides 2,6-difluoroaniline with high selectivity.

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