Cas 1323976-15-3,(4-methyl-5-phenyl-3-(3,4,5-trimethoxyphenyl)-1H-pyrrol-2-yl)(phenyl)methanone

1323976-15-3

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Basic information

Product Name: (4-methyl-5-phenyl-3-(3,4,5-trimethoxyphenyl)-1H-pyrrol-2-yl)(phenyl)methanone
Synonyms: (4-methyl-5-phenyl-3-(3,4,5-trimethoxyphenyl)-1H-pyrrol-2-yl)(phenyl)methanone
CAS NO:1323976-15-3
Molecular Formula:
Molecular Weight: 427.5
EINECS: N/A
Product Categories: N/A
Mol File: 1323976-15-3.mol
Article Data: 1

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: (4-methyl-5-phenyl-3-(3,4,5-trimethoxyphenyl)-1H-pyrrol-2-yl)(phenyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (4-methyl-5-phenyl-3-(3,4,5-trimethoxyphenyl)-1H-pyrrol-2-yl)(phenyl)methanone(1323976-15-3)
EPA Substance Registry System: (4-methyl-5-phenyl-3-(3,4,5-trimethoxyphenyl)-1H-pyrrol-2-yl)(phenyl)methanone(1323976-15-3)

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: 1323976-15-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1323976-15-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,3,9,7 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1323976-15:
(9*1)+(8*3)+(7*2)+(6*3)+(5*9)+(4*7)+(3*6)+(2*1)+(1*5)=163
163 % 10 = 3
So 1323976-15-3 is a valid CAS Registry Number.

1323976-15-3Upstream product

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1323976-15-3Relevant articles and documents

Three-component synthesis of polysubstituted pyrroles from α-diazoketones, nitroalkenes, and amines

Hong, Deng,Zhu, Yuanxun,Li, Yao,Lin, Xufeng,Lu, Ping,Wang, Yanguang

supporting information; experimental part, p. 4668 - 4671 (2011/10/30)

Polysubstituted pyrroles are regiospecifically synthesized via the copper-catalyzed three-component reaction of α-diazoketones, nitroalkenes, and amines under aerobic conditions. The cascade process involves an N-H insertion of carbene, a copper-catalyzed

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