Cas 1426129-85-2,5-(3-chloro-4-methylphenyl)-4-[2-(3-chloro-4-methylphenyl)-2-oxoethyl]-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester

1426129-85-2

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Basic information

Product Name: 5-(3-chloro-4-methylphenyl)-4-[2-(3-chloro-4-methylphenyl)-2-oxoethyl]-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester
Synonyms: 5-(3-chloro-4-methylphenyl)-4-[2-(3-chloro-4-methylphenyl)-2-oxoethyl]-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester
CAS NO:1426129-85-2
Molecular Formula:
Molecular Weight: 444.358
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-(3-chloro-4-methylphenyl)-4-[2-(3-chloro-4-methylphenyl)-2-oxoethyl]-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-(3-chloro-4-methylphenyl)-4-[2-(3-chloro-4-methylphenyl)-2-oxoethyl]-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester(1426129-85-2)
EPA Substance Registry System: 5-(3-chloro-4-methylphenyl)-4-[2-(3-chloro-4-methylphenyl)-2-oxoethyl]-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester(1426129-85-2)

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HazardClass: N/A
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Hazardous Substances Data: 1426129-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1426129-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,1,2 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1426129-85:
(9*1)+(8*4)+(7*2)+(6*6)+(5*1)+(4*2)+(3*9)+(2*8)+(1*5)=152
152 % 10 = 2
So 1426129-85-2 is a valid CAS Registry Number.

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1426129-85-2Relevant academic research and scientific papers

InCl3 catalysed one-pot synthesis of substituted pyrroles and 2-pyrones

Mahato, Sanjit K.,Vinayagam, Jayaraman,Dey, Sumit,Timiri, Ajay K.,Chatterjee, Sourav,Jaisankar, Parasuraman

, p. 241 - 251 (2013/04/23)

An efficient InCl3 catalysed one-pot strategy has been developed for the synthesis of tetra-substituted pyrroles and tri-substituted 2-pyrones in very good yields. Tetra-substituted pyrroles were prepared from 1,4-enediones and β-dicarbonyls employing NH4

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