143956-10-9

Basic information

• Product Name: (2S,5R)-1-Benzoyl-2-tert-butyl-3,5-dimethyl-tetrahydro-pyrimidin-4-one
• CAS NO: 143956-10-9
• Molecular Weight: 288.39
• Mol File: 143956-10-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,5R)-1-Benzoyl-2-tert-butyl-3,5-dimethyl-tetrahydro-pyrimidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,5R)-1-Benzoyl-2-tert-butyl-3,5-dimethyl-tetrahydro-pyrimidin-4-one(143956-10-9)
• EPA Substance Registry System: (2S,5R)-1-Benzoyl-2-tert-butyl-3,5-dimethyl-tetrahydro-pyrimidin-4-one(143956-10-9)

Safety Data

• Hazardous Substances Data: 143956-10-9(Hazardous Substances Data)

Upstream product

• 630-19-3 pivalaldehyde 
• 131791-76-9 cis-2-tert-butyl-6(S)-potassium carboxylate-perhydropyrimidin-4-one 
• 98-88-4 benzoyl chloride 
• 143870-65-9 1-benzoyl-2(S)-tert-butyl-6(S)-carboxy-perhydropyrimidin-4-one 
• 139119-52-1 1-benzoyl-2(S)-tert-butyl-3-methylperhydropyrimidin-4-one 
• 74-88-4 methyl iodide 

Downstream Products

• 183182-01-6 (2S,5S)-1-Benzoyl-2-tert-butyl-3,5-dimethyl-tetrahydro-pyrimidin-4-one 

Relevant articles and documents

Enantioselective synthesis of β-amino acids. 7. Preparation of enantiopure α-substituted β-amino acids from 1-benzoyl-2(S)-tert-butyl-3-methylperhydropyrimidin-4-one

Inexpensive natural α-amino acid L-asparagine was efficiently converted to either (R)- or (S)-α-alkylated β-amino acids in enantiomerically pure state. The key intermediate in this protocol is the enantiopure N,N-acetal pyrimidinone (S)-1, a masked chiral derivative of β-alanine.