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35008-50-5

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35008-50-5 Usage

General Description

(PHENYLSULFONYL)ACETAMIDE is a chemical compound that belongs to the class of sulfonamides. It is the acetamide derivative of phenylsulfonyl and is commonly used as a building block in organic synthesis. (PHENYLSULFONYL)ACETAMIDE is known for its anti-inflammatory and analgesic properties and is used in the pharmaceutical industry to develop drugs for the treatment of various conditions such as pain, fever, and inflammation. It has a white crystalline appearance and is soluble in organic solvents. Additionally, (PHENYLSULFONYL)ACETAMIDE has been studied for its potential use in the synthesis of various pharmaceutical compounds and is an important intermediate in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 35008-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,0 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35008-50:
(7*3)+(6*5)+(5*0)+(4*0)+(3*8)+(2*5)+(1*0)=85
85 % 10 = 5
So 35008-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3S/c9-8(10)6-13(11,12)7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)

35008-50-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 5g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 25g

  • 1435.0CNY

  • Detail
  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 5g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 25g

  • 1435.0CNY

  • Detail
  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 5g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 25g

  • 1435.0CNY

  • Detail
  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 5g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (L12741)  (Phenylsulfonyl)acetamide, 98+%   

  • 35008-50-5

  • 25g

  • 1435.0CNY

  • Detail

35008-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfonyl)acetamide

1.2 Other means of identification

Product number -
Other names benzenesulfonyl-acetic acid amide

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:35008-50-5 SDS

35008-50-5Relevant articles and documents

Benzenesulfonamide compounds

-

Paragraph 0103; 0113-0115, (2021/04/20)

The present invention provides a benzenesulfonamide compound represented by chemical formula 1 or a biotinylated compound thereof. The compounds of the present invention selectively react with a sulfhydryl group (-SH) having unoxidized cysteine, and do no

Selective ruthenium-catalyzed hydration of nitriles to amides in pure aqueous medium under neutral conditions

Cadierno, Victorio,Francos, Javier,Gimeno, Jose

scheme or table, p. 6601 - 6605 (2009/07/10)

A study was conducted to demonstrate that water-soluble ruthenium(II) complexes can be used as catalysts for the hydration of nitriles in pure aqueous media and under neutral conditions. The hydration of benzonitrile was investigated as a model reaction and the ruthenium precursor was added to a 0.33M aqueous solution of benzonitrile at 100°C, while the reaction was monitored by gas chromatography. All the complexes checked, were found to be active and selective catalysts in the hydration process, providing benzamide as a specific reaction product. The most relevant results were obtained by using ruthenium complexes, bearing a nitrogen-containing ligand, which led to appropriate production of benzamide. The most effective ruthenium complex was found to be an efficient catalyst for the selective hydration of a large number of other nitriles.

Efficient lactam synthesis

-

, (2008/06/13)

Lactams, libraries of lactams, and an efficient method of synthesizing a lactam, including a γ-lactam, in which an a-diazoacetamide of the general structure (I) is reacted under conditions promoting intramolecular C-H insertion, for example in the presenc

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