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N-Tosylcarbamic acid isobutyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32363-27-2

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32363-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32363-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,6 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32363-27:
(7*3)+(6*2)+(5*3)+(4*6)+(3*3)+(2*2)+(1*7)=92
92 % 10 = 2
So 32363-27-2 is a valid CAS Registry Number.

32363-27-2SDS

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 2-methylpropyl N-(4-methylphenyl)sulfonylcarbamate

1.2 Other means of identification

Product number -
Other names N-Tosylcarbamic acid isobutyl ester

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:32363-27-2 SDS

32363-27-2Downstream Products

32363-27-2Relevant academic research and scientific papers

Microwave Promoted Transcarbamylation Reaction of Sulfonylcarbamates under Continuous-Flow Conditions

Kumpina, Ilze,Isaksson, Rebecka,S?vmarker, Jonas,Wannberg, Johan,Larhed, Mats

, p. 440 - 445 (2016/03/04)

Successful conditions for the transcarbamylation/transesterification reaction of sulfonylcarbamates with alcohols by microwave heating under continuous-flow conditions were developed. After optimization of the processes, two series of O-alkylsulfonylcarbamates were obtained in high yields and purities using microwave transparent borosilicate tube reactors. In order to also illustrate the usefulness of the protocol in a medicinal chemistry context, the methodology was used for the synthesis of three angiotensin II type 2 receptor ligands.

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