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20228-87-9

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20228-87-9 Usage

General Description

Benzenesulfonamide, N-(cyanomethyl)-4-methyl- is a chemical compound with the molecular formula C9H10N2O2S. It is known for its antimicrobial properties and is commonly used in the synthesis of various pharmaceuticals and drugs. Benzenesulfonamide, N-(cyanomethyl)-4-methyl- is also used as an intermediate in the production of dyes, pigments, and other organic compounds. Its cyanomethyl group enables it to form strong bonds with certain biological molecules, making it useful in the development of antibacterial and antifungal agents. Additionally, this chemical has potential applications in the field of materials science and organic chemistry due to its versatile reactivity and ability to participate in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 20228-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,2 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20228-87:
(7*2)+(6*0)+(5*2)+(4*2)+(3*8)+(2*8)+(1*7)=79
79 % 10 = 9
So 20228-87-9 is a valid CAS Registry Number.

20228-87-9SDS

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 N-(cyanomethyl)-4-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-Cyanomethyl-4-methyl-benzenesulfonamide

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:20228-87-9 SDS

20228-87-9Relevant articles and documents

Transition-Metal-Free α Csp3?H Cyanation of Sulfonamides

Zhou, Liejin,Wei, Siqi,Lei, Ziran,Zhu, Gangguo,Zhang, Zuxiao

, p. 7103 - 7107 (2021/04/16)

This report describes the site-selective α-functionalization of sulfonylamide derivatives through the in-situ generation of imine intermediates. The N?F sulfonylamides, which could facilitate the elimination to generate imines, are coupled with TBACN to e

The use of oxadiazole and triazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 1: Establishing the pharmacophore

Johns, Brian A.,Weatherhead, Jason G.,Allen, Scott H.,Thompson, James B.,Garvey, Edward P.,Foster, Scott A.,Jeffrey, Jerry L.,Miller, Wayne H.

scheme or table, p. 1802 - 1806 (2009/12/01)

A series of HIV-1 integrase inhibitors containing a novel metal binding motif consisting of the 8-hydroxy-1,6-naphthyridine core and either an oxadiazole or triazole has been identified. The design of the key structural components was based on a two-metal

Benzotriazole-assisted synthesis of N-(α-cyanoalkyl)sulfonamides

Katritzky, Alan R.,Oniciu, Daniela C.,Ghiviriga, Ion

, p. 907 - 922 (2007/10/03)

N-(α-benzotriazol-1-ylalkyl)sulfonamides, readily available from benzotriazole, an aldehyde and a sulfonamide, are converted into the corresponding N-(α-cyanoalkyl)sulfonamides in good yields by treatment with potassium cyanide.

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