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123477-57-6

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123477-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123477-57-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,7 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123477-57:
(8*1)+(7*2)+(6*3)+(5*4)+(4*7)+(3*7)+(2*5)+(1*7)=126
126 % 10 = 6
So 123477-57-6 is a valid CAS Registry Number.

123477-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-ynyl pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-PYRROLIDINECARBOXYLIC ACID 2-PROPYNYL 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:123477-57-6 SDS

123477-57-6Downstream Products

123477-57-6Relevant articles and documents

A mild and selective method for N-dealkylation of tertiary amines

Bhat, Ramakrishna G.,Ghosh, Yagnaseni,Chandrasekaran, Srinivasan

, p. 7983 - 7985 (2007/10/03)

Alkyl groups can be cleaved efficiently and selectively from tertiary alkyl amines using propargyl chloroformate. The propargyloxycarbonyl (Poc) protected secondary amines thus obtained can be deblocked under neutral and mild conditions using benzyltriethylammonium tetrathiomolybdate. The generality and compatibility of the method have been studied with a wide range of functionalities. Alkyl groups can be cleaved efficiently and selectively from tertiary alkyl amines using propargyl chloroformate. The propargyloxycarbonyl (Poc) protected secondary amines thus obtained can be deblocked under neutral and mild conditions using benzyltriethylammonium tetrathiomolybdate. The generality and compatibility of the method have been studied with a wide range of functionalities.

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