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L-Proline, 4-methyl-5-oxo-, ethyl ester, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

647856-76-6

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647856-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 647856-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,7,8,5 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 647856-76:
(8*6)+(7*4)+(6*7)+(5*8)+(4*5)+(3*6)+(2*7)+(1*6)=216
216 % 10 = 6
So 647856-76-6 is a valid CAS Registry Number.

647856-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2S,4S)-4-methylpyroglutamate

1.2 Other means of identification

Product number -
Other names (2S,4S)-4-Methyl-5-oxo-pyrrolidine-2-carboxylic acid ethyl 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:647856-76-6 SDS

647856-76-6Downstream Products

647856-76-6Relevant academic research and scientific papers

An alternative to the use of delta-lactam urethanes in the "ring switch" approach to higher homologues of AMPA-type glutamate antagonists.

Hitchcock, Peter B,Masood, Shazia Rahman,Young, Douglas W

, p. 2682 - 2688 (2003)

In an alternative strategy to the use of delta-lactam urethanes for the preparation of homologues of AMPA-type glutamate antagonists, we have used 5-exomethylene derivatives of pyroglutamate esters. The homochiral pyrazole amino acid derivatives 18 and 19 have been prepared in this way. Although this synthesis yields products with a glycine residue separated from a heterocyclic ring by two carbon atoms, the substitution of the heterocyclic ring is different from that in compounds prepared from delta-lactam urethanes. The branched chain compounds 32 and 33 have also been prepared in this way but the second chiral centre is epimerised during the synthesis. An interesting reaction, giving the pyridone 27 from the imino ether 24 and tert-butyl acetoacetate, is also reported.

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