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36556-56-6

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36556-56-6 Usage

Chemical Properties

off-white to greenish-grey low melting solid

Check Digit Verification of cas no

The CAS Registry Mumber 36556-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36556-56:
(7*3)+(6*6)+(5*5)+(4*5)+(3*6)+(2*5)+(1*6)=136
136 % 10 = 6
So 36556-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClF2N/c7-6-4(9)1-3(8)2-5(6)10/h1-2H,10H2

36556-56-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H50363)  2-Chloro-4,6-difluoroaniline, 98%   

  • 36556-56-6

  • 1g

  • 396.0CNY

  • Detail
  • Alfa Aesar

  • (H50363)  2-Chloro-4,6-difluoroaniline, 98%   

  • 36556-56-6

  • 5g

  • 1983.0CNY

  • Detail

36556-56-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-4,6-Difluoroaniline

1.2 Other means of identification

Product number -
Other names 2-CHLORO-4,6-DIFLUOROANILINE

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:36556-56-6 SDS

36556-56-6Relevant articles and documents

Preparation method of 3,5-difluorochlorobenzene

-

Paragraph 0017; 0018; 0019; 0020; 0021; 0022, (2017/08/31)

The invention discloses a preparation method of 3,5-difluorochlorobenzene, and relates to the field of organic synthesis technology. The preparation method comprises the following steps: using 2,4-difluoroaniline as a raw material, introducing chlorine into a meta-position of a benzene ring of fluorine under the limit of an amino group, and then removing amino from the benzene ring to obtain 3,5-difluorochlorobenzene. In the whole preparation process, high temperature and high pressure reaction are avoided, reaction conditions are mild, and intermediates are not required to be separated and purified, and can be directly used in reaction in a next step, so that not only can the treatment cost of the intermediates be reduced, but also the loss of yield of the intermediates caused in the purification process can be reduced, and the conversion percent of the intermediates in amino removal reaction is increased. The molar yield of the product, 3,5-difluorochlorobenzene, produced by using the method can be up to 80% and more and the purity can be up to 99.5% or more, so that the yield and purity of the product are ensured on the basis of reducing the cost of preparation, and the product, 3,5-difluorochlorobenzene, is used as a drug intermediate for preparation of drug.

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