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D-Proline, 3-hydroxy-4-methyl-2-[(1S)-2-methyl-1-(phenylmethoxy)propyl]-5-oxo-, (3S,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

876952-15-7

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876952-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876952-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,9,5 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 876952-15:
(8*8)+(7*7)+(6*6)+(5*9)+(4*5)+(3*2)+(2*1)+(1*5)=227
227 % 10 = 7
So 876952-15-7 is a valid CAS Registry Number.

876952-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,4R)-2-((S)-1-benzoyloxy-2-methyl-propyl)-3-hydroxy-4-methyl-5-oxo-pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:876952-15-7 SDS

876952-15-7Relevant articles and documents

Enantioselective total syntheses of (-)-clasto-lactacystin β-lactone and 7-epi-(-)-clasto-lactacystin β-lactone

Hayes, Christopher J.,Sherlock, Alexandra E.,Selby, Matthew D.

, p. 193 - 195 (2007/10/03)

An alkylidene carbene 1,5-CH insertion has been used as a key step in an efficient enantioselective total synthesis of (-)-clasto-lactacystin β-lactone, and its C7-epimer. An additional noteworthy feature of the synthesis is the use of a novel oxidative deprotection procedure, utilizing DMDO, for the conversion of a late-stage benzylidene acetal into a primary alcohol and a secondary benzoate ester. The Royal Society of Chemistry 2006.

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