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2729-36-4

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2729-36-4 Usage

Uses

3,4-Dichloro-6-fluoroaniline is used as pharmaceutical intermediates

Check Digit Verification of cas no

The CAS Registry Mumber 2729-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2729-36:
(6*2)+(5*7)+(4*2)+(3*9)+(2*3)+(1*6)=94
94 % 10 = 4
So 2729-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl2FN/c7-3-1-5(9)6(10)2-4(3)8/h1-2H,10H2

2729-36-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H59506)  3,4-Dichloro-6-fluoroaniline, 96%   

  • 2729-36-4

  • 250mg

  • 1483.0CNY

  • Detail
  • Alfa Aesar

  • (H59506)  3,4-Dichloro-6-fluoroaniline, 96%   

  • 2729-36-4

  • 1g

  • 5412.0CNY

  • Detail

2729-36-4SDS

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 4,5-dichloro-2-fluoroaniline

1.2 Other means of identification

Product number -
Other names 4,5-dichloro-2-fluoro-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:2729-36-4 SDS

2729-36-4Relevant articles and documents

Cobalt in N-doped carbon matrix catalyst for chemoselective hydrogenation of nitroarenes

Dai, Yihu,Jiang, Chunyang,Xu, Min,Bian, Bo,Lu, Di,Yang, Yanhui

, p. 158 - 166 (2019/06/03)

Anilines as important intermediates for both organic synthesis and industrial manufactory are densely substituted with a variety of functional moieties, and the transformation of nitroarenes into corresponding anilines requires catalytically selective hydrogenation catalyst. Herein, we describe a simple pyrolysis strategy to prepare cobalt catalysts in nitrogen-doped carbon matrix applied in the selective hydrogenation of nitroarenes with molecular hydrogen. The Co/NC catalysts are obtained through thermal treatment of mixed precursors of cobalt phthalocyanine and melamine. The surface-modified Co particles with Co3O4 and CoNx sites are surrounded by N-doped carbon layers according to a series of structural characterization results. These Co/NC catalysts are capable of efficiently selective hydrogenation of nitrobenzene and various substituted nitroarenes into corresponding anilines under relatively mild reaction conditions. The optimal catalytic hydrogenation performance is contributed to the fast rate of H2 dissociated activation on the CoNx active sites and the facile adsorption of the reactant substances, which is verified by the isotopic H2-D2 exchange experiments, reactant adsorption and the ORR reaction tests. Furthermore, the heterogeneous Co/NC catalyst is highly stable without the Co leaching and deactivation issues during the recycling reaction runs.

METHODS AND USE OF BIFUNCTIONAL ENZYME-BUILDING CLAMP-SHAPED MOLECULES

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Page/Page column 42; 43, (2012/10/07)

This invention is in the fields of cancer therapy. More particularly it concerns compounds which are useful agents for inhibiting cell proliferative disorders, especially those disorders characterized by over activity and/or inappropriate activity of a EG

Epidermal growth factor receptor binding compounds for positron emission tomography

-

, (2008/06/13)

A radiolabeled compound of a formula: is described. R1 and R2 are each independently selected from the group consisting of hydrogen, alkyl, hydroxy, alkoxy, halo, haloalkyl, carboxy, carbalkoxy and salts thereof; and A, B, C and D are each independently s

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