Cas 1426129-80-7,2-[4-acetyl-2-(4-chlorophenyl)-5-methyl-1H-pyrrol-3-yl]-1-(4-chlorophenyl)ethanone

1426129-80-7

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Basic information

Product Name: 2-[4-acetyl-2-(4-chlorophenyl)-5-methyl-1H-pyrrol-3-yl]-1-(4-chlorophenyl)ethanone
Synonyms: 2-[4-acetyl-2-(4-chlorophenyl)-5-methyl-1H-pyrrol-3-yl]-1-(4-chlorophenyl)ethanone
CAS NO:1426129-80-7
Molecular Formula:
Molecular Weight: 386.277
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: 2-[4-acetyl-2-(4-chlorophenyl)-5-methyl-1H-pyrrol-3-yl]-1-(4-chlorophenyl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2-[4-acetyl-2-(4-chlorophenyl)-5-methyl-1H-pyrrol-3-yl]-1-(4-chlorophenyl)ethanone(1426129-80-7)
EPA Substance Registry System: 2-[4-acetyl-2-(4-chlorophenyl)-5-methyl-1H-pyrrol-3-yl]-1-(4-chlorophenyl)ethanone(1426129-80-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1426129-80-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1426129-80-7 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 1426129-80:
(9*1)+(8*4)+(7*2)+(6*6)+(5*1)+(4*2)+(3*9)+(2*8)+(1*0)=147
147 % 10 = 7
So 1426129-80-7 is a valid CAS Registry Number.

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1426129-80-7Relevant 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)

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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