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147332-08-9

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147332-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147332-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,3,3 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 147332-08:
(8*1)+(7*4)+(6*7)+(5*3)+(4*3)+(3*2)+(2*0)+(1*8)=119
119 % 10 = 9
So 147332-08-9 is a valid CAS Registry Number.

147332-08-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-pyrrolidine-2,3-dicarboxylic 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:147332-08-9 SDS

147332-08-9Downstream Products

147332-08-9Relevant articles and documents

Stereoselective synthesis of conformationally restricted analogues of aspartic and glutamic acids front endocyclic enecarbamates

Carpes, Marcos Jose S.,Miranda, Paulo Cesar M. L.,Correia, Carlos Roque D.

, p. 1869 - 1872 (2007/10/03)

The stereoselective synthesis of cyclic amino acids incorporating the care framework of aspartic acid and glutamic acids were accomplished from a common intermediate. Oxidative cleavage of an aza-bicyclic-dichlorocyclobutanone/pentanone with Me2CuLi/Ac2O followed by ozonolysis furnished the amino acid derivatives in good overall yields in a three-step sequence. This protocol was also applied to the synthesis of a cis-β-amino acid and to the enantioselective construction of a chimeric amino acid incorporating the basic skeleton of four different naturally occurring amino acids into a single structure.

Generation of α-amino acid homoenolate equivalents. Synthesis of 3-substituted prolines

Moss, William O.,Bradbury, Roben H.,Hales, Neil J.,Gallagher, Timothy

, p. 5653 - 5656 (2007/10/02)

Deprotonation of the N-protected aminoketene-S,S-acetal (6) and reaction of allylic anion (7) with electrophiles leads to adducts (8) which have been converted to 3-substituted prolines (11). Conformationally constrained variants (11d) and (11e) of aspartic and glutamic acid have been prepared.

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