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1197193-21-7

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1197193-21-7 Usage

Uses

4-Fluoro-2-(methylsulfonyl)aniline acts as a reagent in the synthesis of indoleacetic acid diazine derivative as potent, selective, and orally bioavailable antagonists of CRTH2 for the treatment of allergic inflammatory diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1197193-21-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,1,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1197193-21:
(9*1)+(8*1)+(7*9)+(6*7)+(5*1)+(4*9)+(3*3)+(2*2)+(1*1)=177
177 % 10 = 7
So 1197193-21-7 is a valid CAS Registry Number.

1197193-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-2-(methylsulfonyl)aniline

1.2 Other means of identification

Product number -
Other names 4-fluoro-2-methylsulfonylaniline

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:1197193-21-7 SDS

1197193-21-7Downstream Products

1197193-21-7Relevant articles and documents

4 - Fluorine substituted aryl amine compound and synthesis method thereof

-

Paragraph 0075-0077, (2021/09/22)

The invention discloses a synthesis method of 4 -fluorine substituted aryl amine compound, which comprises the following steps: 1) taking acyl-protected phenylhydroxylamine as a substrate, and generating 4 -fluorine substituted aniline compound under basic conditions by taking sulfonyl fluoride as a fluorine source in a polar solvent. 2) The deprotection is carried out under dilute acid conditions or Pd by catalytic hydrogenation to give the 4 - fluorine-substituted aryl amine compound. 4 - Fluorine substituted aniline compounds which are synthesized by the invention greatly increase the lipophilic property due to the introduction of fluorine atoms, and can be widely applied to preparation of fluorine-containing drugs and pesticide and dye intermediates. , The adopted raw materials are industrial products, are cheap and easily available, and are commercially available. 4 - Fluoroaryl aniline prepared by the method is high in yield, and the product with the purity 90% can be obtained in a yield of more than ≥ 99%. The method is simple to operate and low in cost, is very suitable for industrialization, and can be widely popularized and used.

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