Cas 1351353-89-3,((5S,6S,7R)-5-(3-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol

1351353-89-3

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Basic information

Product Name: ((5S,6S,7R)-5-(3-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol
Synonyms: ((5S,6S,7R)-5-(3-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol
CAS NO:1351353-89-3
Molecular Formula:
Molecular Weight: 335.406
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: ((5S,6S,7R)-5-(3-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol(CAS DataBase Reference)
NIST Chemistry Reference: ((5S,6S,7R)-5-(3-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol(1351353-89-3)
EPA Substance Registry System: ((5S,6S,7R)-5-(3-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol(1351353-89-3)

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: 1351353-89-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1351353-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,1,3,5 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1351353-89:
(9*1)+(8*3)+(7*5)+(6*1)+(5*3)+(4*5)+(3*3)+(2*8)+(1*9)=143
143 % 10 = 3
So 1351353-89-3 is a valid CAS Registry Number.

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1351353-89-3Relevant academic research and scientific papers

Organocatalytic asymmetric domino aza-michael - Mannich reaction: Synthesis of tetrahydroimidazopyrimidine derivatives

Li, Hong,Zhao, Junling,Zeng, Lili,Hu, Wenhui

, p. 8064 - 8069 (2011/11/28)

Highly substituted tetrahydroimidazopyrimidine derivatives with three chiral centers have been synthesized for the first time using an organocatalytic asymmetric domino aza-Michael - Mannich reaction of α,β-unsaturated aldehydes and N-arylidene-1H-imidazo

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