Cas 1268627-82-2,1,3-dibenzyl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)tetrahydropyrimidin-4(1H)-one

1268627-82-2

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Basic information

Product Name: 1,3-dibenzyl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)tetrahydropyrimidin-4(1H)-one
Synonyms: 1,3-dibenzyl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)tetrahydropyrimidin-4(1H)-one
CAS NO:1268627-82-2
Molecular Formula:
Molecular Weight: 547.697
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: 1,3-dibenzyl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)tetrahydropyrimidin-4(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-dibenzyl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)tetrahydropyrimidin-4(1H)-one(1268627-82-2)
EPA Substance Registry System: 1,3-dibenzyl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)tetrahydropyrimidin-4(1H)-one(1268627-82-2)

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: 1268627-82-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1268627-82-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,6,2 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1268627-82:
(9*1)+(8*2)+(7*6)+(6*8)+(5*6)+(4*2)+(3*7)+(2*8)+(1*2)=192
192 % 10 = 2
So 1268627-82-2 is a valid CAS Registry Number.

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1268627-82-2Relevant academic research and scientific papers

FeCl3·6H2O-promoted skeleton-rearrangement of 1-substituted-3-benzazepines: Substrate extension and product utilization

Zhang, Jing,Wu, Kui,Wang, Meining,Jiang, Jianqin,Zhang, Ao

experimental part, p. 842 - 848 (2011/03/19)

FeCl3·6H2O-promoted skeleton-rearrangement of 1-substituted-3-benzazepines was further exploited. Both 1-aryl- and 1-alkyl- or 1-alkenyl-benzazepines underwent this reaction smoothly. The rearrangement products were used to prepare a

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