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108128-27-4

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108128-27-4 Usage

General Description

1-(Phenylsulfonyl)pyrazole is a chemical compound with the molecular formula C11H9N3O2S. It is a pyrazole derivative substituted with a phenylsulfonyl group at the 1-position. 1-(PHENYLSULFONYL)PYRAZOLE has been studied for its potential applications in medicinal chemistry due to its diverse biological activities, including anti-inflammatory and antinociceptive effects. Additionally, 1-(phenylsulfonyl)pyrazole has been investigated for its potential use as a fungicide and herbicide due to its inhibitory effects on certain enzyme targets. Its unique structure and biological activities make it a promising compound for further research and potential development in pharmaceutical and agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 108128-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,2 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108128-27:
(8*1)+(7*0)+(6*8)+(5*1)+(4*2)+(3*8)+(2*2)+(1*7)=104
104 % 10 = 4
So 108128-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2S/c12-14(13,11-8-4-7-10-11)9-5-2-1-3-6-9/h1-8H

108128-27-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H32914)  1-Phenylsulfonylpyrazole, 95%   

  • 108128-27-4

  • 250mg

  • 948.0CNY

  • Detail
  • Alfa Aesar

  • (H32914)  1-Phenylsulfonylpyrazole, 95%   

  • 108128-27-4

  • 1g

  • 2636.0CNY

  • Detail

108128-27-4SDS

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 1-(benzenesulfonyl)pyrazole

1.2 Other means of identification

Product number -
Other names 1-Benzenesulfonylpyrazole

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:108128-27-4 SDS

108128-27-4Downstream Products

108128-27-4Relevant articles and documents

METHODS FOR THE PREPARATION OF 5-BROMO-2-(3-CHLORO-PYRIDIN-2-YL)-2H-PYRAZOLE-3-CARBOXYLIC ACID

-

Paragraph 0244; 0245, (2021/04/23)

Described herein are novel methods of synthesizing 5-Bromo-2-(3-chloro-pyridin-2-yl)- 2H-pyrazole-3-carboxylic acid from pyrazole or pyrazole derivatives. Also described herein are novel reaction intermediates.

Sulfonamide Synthesis through Electrochemical Oxidative Coupling of Amines and Thiols

Laudadio, Gabriele,Barmpoutsis, Efstathios,Schotten, Christiane,Struik, Lisa,Govaerts, Sebastian,Browne, Duncan L.,No?l, Timothy

supporting information, p. 5664 - 5668 (2019/04/17)

Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous development of novel and efficient synthetic methods to access these functional groups. Herein, we report an environmentally benign electrochemical method which enables the oxidative coupling between thiols and amines, two readily available and inexpensive commodity chemicals. The transformation is completely driven by electricity, does not require any sacrificial reagent or additional catalysts and can be carried out in only 5 min. Hydrogen is formed as a benign byproduct at the counter electrode. Owing to the mild reaction conditions, the reaction displays a broad substrate scope and functional group compatibility.

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