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1H-Pyrrole-2-carboxylic acid, 5,5'-(phenylmethylene)bis[3-ethyl-4-methyl- is a complex organic compound with the molecular formula C22H22N2O4. It is a derivative of pyrrole-2-carboxylic acid, featuring a phenylmethylene bridge connecting two 3-ethyl-4-methyl-1H-pyrrole-2-carboxylic acid units. 1H-Pyrrole-2-carboxylic acid, 5,5'-(phenylmethylene)bis[3-ethyl-4-methyl- is characterized by its unique structure, which includes two pyrrole rings, each with an ethyl and methyl substituent, and a phenyl group in the middle. It is likely to be used in the synthesis of various organic compounds, pharmaceuticals, or as a building block in materials science due to its potential to form stable complexes with metal ions. The compound's specific applications and properties would depend on its reactivity and stability, which are influenced by its molecular structure.

87597-48-6

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87597-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87597-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,9 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87597-48:
(7*8)+(6*7)+(5*5)+(4*9)+(3*7)+(2*4)+(1*8)=196
196 % 10 = 6
So 87597-48-6 is a valid CAS Registry Number.

87597-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(5-carboxy-4-ethyl-3-methyl-2-pyrryl)phenylmethan

1.2 Other means of identification

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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

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More Details:87597-48-6 SDS

87597-48-6Relevant academic research and scientific papers

Synthesis of 5,15-Diaryl-Substituted Porphyrins by Aminomethylation of Bis(4-ethyl-3-methyl-2-pyrryl)phenylmethanes

Hombrecher, Hermann K.,Horter, Gaby

, p. 219 - 227 (2007/10/02)

The synthesis of unsymmetrically diarylsubstituted porphyrins 11a-g (yields 5-19 percent) is described.Aminomethylation of dipyrromethane 6a with Mannich reagent 9 in acetonitrile leads to the intermediate 10, which is directly converted into the porphyri

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