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1,2-Pyrrolidinedicarboxylic acid, 3-(2-methoxy-2-oxoethyl)-4-[1-methylene-4-oxo-3-(phenylthio)pentyl]-, 1-ethyl 2-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87696-37-5

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87696-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87696-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,9 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87696-37:
(7*8)+(6*7)+(5*6)+(4*9)+(3*6)+(2*3)+(1*7)=195
195 % 10 = 5
So 87696-37-5 is a valid CAS Registry Number.

87696-37-5SDS

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 ethyl methyl (2S,3S,4S)-3-<(methoxycarbonyl)methyl>-4-<1-<3-oxo-2-(phenylthio)butyl>vinyl>-1,2-pyrrolidinedicarboxylate

1.2 Other means of identification

Product number -
Other names (2S,3S,4S)-3-Methoxycarbonylmethyl-4-(1-methylene-4-oxo-3-phenylsulfanyl-pentyl)-pyrrolidine-1,2-dicarboxylic acid 1-ethyl ester 2-methyl 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:87696-37-5 SDS

87696-37-5Downstream Products

87696-37-5Relevant academic research and scientific papers

Pelladium(II)-Catalyzed Olefin-Coupling Reactions of Kainic Acid: Effects of Substitution on the Isopropenyl Group on Receptor Binding

Convay, Gregory A.,Park, Joon Sup,Maggiora, Linda,Mertes, Mathias P.,Galton, Noemi,Michaelis, Elias K.

, p. 52 - 56 (2007/10/02)

Two palladium-catalyzed carbon-carbon bond forming reactions were found to be useful for the modification of a protected amino acid derivative containing a sterically hindered isopropenyl group.Arylation of the terminal methylene group of the dimethyl est

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