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N-[4-(4-Fluorophenylsulphonyl)phenyl]acetamide is a chemical compound with the molecular formula C14H12FNO3S. It is an organic molecule that features a sulphonyl group (-SO2-) connecting two phenyl rings, one of which is substituted with a fluorine atom. The compound also contains an amide group (-CONH2) attached to the second phenyl ring. This specific structure may confer unique chemical properties and reactivity, making it potentially useful in various applications such as pharmaceuticals, materials science, or as a chemical intermediate in the synthesis of more complex molecules. The presence of the fluorine atom can significantly influence the compound's electronic properties and metabolic stability, which is often a consideration in drug design.

734-22-5

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734-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 734-22-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 734-22:
(5*7)+(4*3)+(3*4)+(2*2)+(1*2)=65
65 % 10 = 5
So 734-22-5 is a valid CAS Registry Number.

734-22-5SDS

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 N-[4-(4-fluorophenyl)sulfonylphenyl]acetamide

1.2 Other means of identification

Product number -
Other names (4-Acetamino-phenyl)-(4-fluor-phenyl)-sulfon

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:734-22-5 SDS

734-22-5Downstream Products

734-22-5Relevant academic research and scientific papers

Complementary Site-Selective Sulfonylation of Aromatic Amines by Superacid Activation

Bourbon, Paul,Appert, Emeline,Martin-Mingot, Agnès,Michelet, Bastien,Thibaudeau, Sébastien

, p. 4115 - 4120 (2021/06/21)

Under superacidic conditions, aniline and indole derivatives are sulfonylated at low temperature with easy-to-access arenesulfonic acids or arenesulfonyl hydrazides. By modification of the functional-group directing effect through protonation, this method allows nonclassical site functionalization by overcoming the innate regioselectivity of electrophilic aromatic substitution. This superacid-mediated sulfonylation of arenes is complementary to existing methods and can be applied, through protection by protonation, to the late-stage site-selective functionalization of natural alkaloids and active pharmaceutical ingredients.

2-Amino-4'(phenylsulfonyl) acetanilides

-

, (2008/06/13)

A method of modulating the immune response system in a warm-blooded animal by the administration of N-substituted-phenylthioanilines, N-substituted-phenylsulfinylanilines, and N-substituted-phenylsulfonylanilines, certain of which are new compounds.

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