Cas 1332482-16-2,(5S,6S,7R)-5-(4-nitrophenyl)-7-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde

1332482-16-2

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Basic information

Product Name: (5S,6S,7R)-5-(4-nitrophenyl)-7-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde
Synonyms: (5S,6S,7R)-5-(4-nitrophenyl)-7-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde
CAS NO:1332482-16-2
Molecular Formula:
Molecular Weight: 416.359
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-(4-nitrophenyl)-7-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (5S,6S,7R)-5-(4-nitrophenyl)-7-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde(1332482-16-2)
EPA Substance Registry System: (5S,6S,7R)-5-(4-nitrophenyl)-7-(4-(trifluoromethyl)phenyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde(1332482-16-2)

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: 1332482-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1332482-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,4,8 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1332482-16:
(9*1)+(8*3)+(7*3)+(6*2)+(5*4)+(4*8)+(3*2)+(2*1)+(1*6)=132
132 % 10 = 2
So 1332482-16-2 is a valid CAS Registry Number.

1332482-16-2Upstream product

1332482-16-2Downstream Products

1351362-06-5 ((5S,6S,7R)-5-(4-nitrophenyl)-7-[4-(trifluoromethyl)phenyl]-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol

1332482-16-2Relevant academic research and scientific papers

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

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

experimental part, 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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