1332482-02-6

Basic information

• Product Name: (5S,6S,7R)-5-(3-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde
• Synonyms: (5S,6S,7R)-5-(3-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde
• CAS NO: 1332482-02-6
• Molecular Weight: 382.26
• Mol File: 1332482-02-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (5S,6S,7R)-5-(3-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (5S,6S,7R)-5-(3-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde(1332482-02-6)
• EPA Substance Registry System: (5S,6S,7R)-5-(3-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde(1332482-02-6)

Safety Data

• Hazardous Substances Data: 1332482-02-6(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 97985-66-5 3-(3-bromophenyl)prop-2-en-1-al 
• 77302-61-5 N-benzylidene-1H-imidazol-2-amine 

Downstream Products

• 1351353-94-0 ((5S,6S,7R)-5-(3-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 

Relevant articles and documents

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

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