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Cyclohexanesulfonamide, N-methyl-2-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96355-28-1

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96355-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96355-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,5 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96355-28:
(7*9)+(6*6)+(5*3)+(4*5)+(3*5)+(2*2)+(1*8)=161
161 % 10 = 1
So 96355-28-1 is a valid CAS Registry Number.

96355-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-2-oxocyclohexane-1-sulfonamide

1.2 Other means of identification

Product number -
Other names Cyclohexanesulfonamide,N-methyl-2-oxo

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:96355-28-1 SDS

96355-28-1Relevant academic research and scientific papers

Improved method for the synthesis of N-methyl-2-oxoalkanesulfonamides

Vega,Molina,Alajarin,Vaquero,Garcia Navio,Alvarez-Builla

, p. 3677 - 3678 (1992)

A series of N-methyl-2-oxoalkanesulfonamides was prepared by reaction between silyl enol ethers and N-methyl-sulfonylimine. In all cases yields were comparatively higher to those obtained by a previously described procedure.

Synthesis and reactivity of N-alkyl-2-oxoalkanesulfonamides

Vega, Juan A.,Alajarin, Ramon,Vaquero, Juan J.,Alvarez-Builla, Julio

, p. 3589 - 3606 (2007/10/03)

A series of N-alkyl-2-oxoalkanesulfonamides have been synthesized by reacting silyl enol ethers with N-alkyl-sulfamoyl chlorides. Their reactivity towards electrophiles was investigated in order to explore the regio- and stereoselectivity of the process. 2-Oxoalkanesulfonamides were used to prepare 5-(methylsulfamoyl)-1,4-dihydropyridines derivatives.

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