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26630-73-9

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26630-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26630-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,3 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26630-73:
(7*2)+(6*6)+(5*6)+(4*3)+(3*0)+(2*7)+(1*3)=109
109 % 10 = 9
So 26630-73-9 is a valid CAS Registry Number.

26630-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[2-(benzyloxycarbonylamino)ethyl] sulfide

1.2 Other means of identification

Product number -
Other names [2-(2-Benzyloxycarbonylamino-ethylsulfanyl)-ethyl]-carbamic acid benzyl 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:26630-73-9 SDS

26630-73-9Relevant articles and documents

Preparation and characterization of some substituted benzyl n-nitrosocarbamates containing an n-2-(methylthio)ethyl or a bis(2-aminoethyl)sulfide functionality

Venkata, Satya,Shamo, Eric,Benin, Vladimir

experimental part, p. 1406 - 1414 (2009/09/26)

The synthesis and characterization of some substituted benzyl N-nitrosocarbamates with an N-2-(methylthio)ethyl or a bis(2-aminoethyl)sulfide functionality is reported, as a part of a long-term goal to design and prepare novel photolabile structures that could be used as substances for controlled release of alkylating and/or crosslinking agents. The synthesis was accomplished by reaction of benzyl chloroformates with the corresponding amines, resulting in the preparation of carbamates. The latter were subsequently nitrosated, utilizing two different N-nitrosation methods, to yield the target structures.

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