Cas 1245641-17-1,7-(2,4-dichlorobenzylidene)-4-(2,4-dichlorophenyl)-1,3,4,5,6,7-hexahydro-2H-cyclopenta[d]pyrimidin-2-one

1245641-17-1

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Basic information

Product Name: 7-(2,4-dichlorobenzylidene)-4-(2,4-dichlorophenyl)-1,3,4,5,6,7-hexahydro-2H-cyclopenta[d]pyrimidin-2-one
Synonyms: 7-(2,4-dichlorobenzylidene)-4-(2,4-dichlorophenyl)-1,3,4,5,6,7-hexahydro-2H-cyclopenta[d]pyrimidin-2-one
CAS NO:1245641-17-1
Molecular Formula:
Molecular Weight: 440.156
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: 7-(2,4-dichlorobenzylidene)-4-(2,4-dichlorophenyl)-1,3,4,5,6,7-hexahydro-2H-cyclopenta[d]pyrimidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 7-(2,4-dichlorobenzylidene)-4-(2,4-dichlorophenyl)-1,3,4,5,6,7-hexahydro-2H-cyclopenta[d]pyrimidin-2-one(1245641-17-1)
EPA Substance Registry System: 7-(2,4-dichlorobenzylidene)-4-(2,4-dichlorophenyl)-1,3,4,5,6,7-hexahydro-2H-cyclopenta[d]pyrimidin-2-one(1245641-17-1)

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: 1245641-17-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1245641-17-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,6,4 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1245641-17:
(9*1)+(8*2)+(7*4)+(6*5)+(5*6)+(4*4)+(3*1)+(2*1)+(1*7)=141
141 % 10 = 1
So 1245641-17-1 is a valid CAS Registry Number.

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1245641-17-1Relevant academic research and scientific papers

An efficient and environmentally friendly procedure for synthesis of pyrimidinone derivatives by use of a Biginelli-type reaction

Lei, Min,Ma, Lei,Hu, Lihong

, p. 1005 - 1008 (2010)

A Biginelli-type three-component reaction involving cyclopentanone, aromatic aldehyde, and urea or thiourea for preparation of pyrimidinone derivatives under neat conditions is described. This condensation reaction can also take place smoothly in the pres

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