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882739-31-3

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882739-31-3 Usage

Uses

Reactant for oxidative C-H amination reactions

Check Digit Verification of cas no

The CAS Registry Mumber 882739-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,7,3 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 882739-31:
(8*8)+(7*8)+(6*2)+(5*7)+(4*3)+(3*9)+(2*3)+(1*1)=213
213 % 10 = 3
So 882739-31-3 is a valid CAS Registry Number.

882739-31-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Aldrich

  • (680834)  N-(2,2,2-Trichloroethoxysulfonyl)urea  96%

  • 882739-31-3

  • 680834-1G

  • 1,122.03CNY

  • Detail
  • Aldrich

  • (680834)  N-(2,2,2-Trichloroethoxysulfonyl)urea  96%

  • 882739-31-3

  • 680834-5G

  • 4,199.13CNY

  • Detail

882739-31-3SDS

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 2,2,2-trichloroethyl N-carbamoylsulfamate

1.2 Other means of identification

Product number -
Other names Aminocarbonylsulfamic acid,3,3,3-trichloroethoxy 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:882739-31-3 SDS

882739-31-3Downstream Products

882739-31-3Relevant articles and documents

Expanding the substrate scope for C-H amination reactions: Oxidative cyclization of urea and guanidine derivatives

Kim, Mihyong,Mulcahy, John V.,Espino, Christine G.,Du Bois

, p. 1073 - 1076 (2007/10/03)

Oxidative C-H amination of N-trichloroethoxysulfonyl-protected ureas and guanidines is demonstrated to proceed in high yield for tertiary and benzylic-derived substrates. The success of these reactions is predicated on the choice of the electron-withdrawn

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