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1H-Pyrrole-3-acetic acid, 4-methyl-5-[(phenylmethoxy)carbonyl]-2-(trichloromethyl)-, methyl ester is a complex organic compound with the molecular formula C15H14Cl3NO4. It is a derivative of 1H-pyrrole-3-acetic acid, featuring a methyl group at the 4-position, a phenylmethoxycarbonyl group at the 5-position, and a trichloromethyl group at the 2-position. The compound is further characterized by the presence of a methyl ester group, which is attached to the carboxylic acid functionality. This molecule is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique structure and functional groups.

87281-59-2

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87281-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87281-59-2 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 87281-59:
(7*8)+(6*7)+(5*2)+(4*8)+(3*1)+(2*5)+(1*9)=162
162 % 10 = 2
So 87281-59-2 is a valid CAS Registry Number.

87281-59-2SDS

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 4-Methoxycarbonylmethyl-3-methyl-5-trichloromethyl-1H-pyrrole-2-carboxylic acid benzyl ester

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

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More Details:87281-59-2 SDS

87281-59-2Relevant academic research and scientific papers

Neighboring Group Participation in the Pyrrole Series

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

, p. 4296 - 4302 (1983)

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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