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1H-Pyrrole-2-carboxylic acid, 4-(2-cyanoethyl)-3,5-dimethyl-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87281-57-0

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87281-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87281-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,8 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87281-57:
(7*8)+(6*7)+(5*2)+(4*8)+(3*1)+(2*5)+(1*7)=160
160 % 10 = 0
So 87281-57-0 is a valid CAS Registry Number.

87281-57-0SDS

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 benzyl 4-(2-cyanoethyl)-3,5-dimethylpyrrole-2-carboxylate

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:87281-57-0 SDS

87281-57-0Relevant academic research and scientific papers

SYNTHESES OF DERIVATIVES OF PROTOPORPHYRIN-IX REGIOSELECTIVELY ENRICHED IN THE PROPIONIC SIDE CHAINS WITH CARBON-13

Smith, Kevin M.,Pandey, Ravindra K.,Tabba, Hani D.

, p. 3333 - 3357 (2007/10/02)

Using copper(II) promoted cyclizations of 1',8'-dimethyl-a,c-biladiene salts, derivatives of protoporphyrin-IX with regioselectively carbon-13 enriched carboxyl (2, 15) and propionate methylene (3, 20) carbons are synthesized.The source of carbon-13 in th

Neighboring Group Participation in the Pyrrole Series

Smith, Kevin M.,Martynenko, Zoya,Pandey, Ravindra K.,Tabba, Hani D.

, p. 4296 - 4302 (2007/10/02)

With use of proton and carbon-13 NMR spectroscopy of deuterium- and carbon-13-labeled substrates, the transformation of certain (2-hydroxyethyl)pyrroles (4, 18, 21) into the corresponding (2-haloethyl)pyrroles (using thionyl chloride/pyridine or triphenyl

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