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2106-02-7

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2106-02-7 Usage

Chemical Properties

clear orange-brown to brown liquid

Synthesis Reference(s)

The Journal of Organic Chemistry, 39, p. 1758, 1974 DOI: 10.1021/jo00925a037

Check Digit Verification of cas no

The CAS Registry Mumber 2106-02-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2106-02:
(6*2)+(5*1)+(4*0)+(3*6)+(2*0)+(1*2)=37
37 % 10 = 7
So 2106-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClFN/c7-5-3-4(8)1-2-6(5)9/h1-3H,9H2

2106-02-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A15492)  2-Chloro-4-fluoroaniline, 97%   

  • 2106-02-7

  • 5g

  • 249.0CNY

  • Detail
  • Alfa Aesar

  • (A15492)  2-Chloro-4-fluoroaniline, 97%   

  • 2106-02-7

  • 25g

  • 959.0CNY

  • Detail
  • Alfa Aesar

  • (A15492)  2-Chloro-4-fluoroaniline, 97%   

  • 2106-02-7

  • 100g

  • 3198.0CNY

  • Detail

2106-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-4-fluoroaniline

1.2 Other means of identification

Product number -
Other names 2-chloro-4-fluoro-benzenamin

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:2106-02-7 SDS

2106-02-7Relevant articles and documents

-

Mulvey et al.

, p. 1419 (1978)

-

The Bamberger reaction in hydrogen fluoride: the use of mild reductive metals for the preparation of fluoroaromatic amines

Tordeux, Marc,Wakselman, Claude

, p. 251 - 254 (2007/10/03)

The reduction of nitroaromatic compounds by various metals (tin, lead, bismuth) in liquid hydrogen fluoride under an inert atmosphere leads to fluoroaromatic amines, in accord with the Bamberger reaction.Generally, a co-solvent such as pentane or methylene chloride is used.Some non-fluorinated arylamines are also formed by a competitive direct reduction of the N-arylhydroxylamine intermediate.Of the mild reductive metals studied, bismuth was the most selective. - Keywords: Bamberger reaction; Hydrogen fluoride; Mild reductive metals; Fluoroaromatic amines; NMR spectroscopy

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