62143-51-5

Basic information

• Product Name: 2,6-Piperidinedione, 4-phenyl-1-(phenylmethyl)-
• CAS NO: 62143-51-5
• Molecular Formula: C18H17NO2
• Molecular Weight: 279.338
• Mol File: 62143-51-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,6-Piperidinedione, 4-phenyl-1-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Piperidinedione, 4-phenyl-1-(phenylmethyl)-(62143-51-5)
• EPA Substance Registry System: 2,6-Piperidinedione, 4-phenyl-1-(phenylmethyl)-(62143-51-5)

Safety Data

• Hazardous Substances Data: 62143-51-5(Hazardous Substances Data)

Upstream product

• 123-91-1 1,4-dioxane 
• 4165-96-2 3-phenylglutaric acid 
• 100-46-9 benzylamine 
• 6768-26-9 2-phenyl-1,1,3,3-tetraethoxycarbonylpropane 
• 92410-37-2 5-(benzylamino)-5-oxo-3-phenylpentanoic acid 
• 4160-80-9 3-phenylglutaric acid anhydride 

Downstream Products

• 771-99-3 4-phenylpiperidine 
• 19015-37-3 1-(phenylmethyl)-4-phenylpiperidine 

Relevant articles and documents

Enantioselective Desymmetrization of Glutarimides Catalyzed by Oxazaborolidines Derived from cis-1-Amino-indan-2-ol

Enantioselective reductive desymmetrization of glutarimides has been achieved employing an oxazaborolidine catalyst derived from cis-1-amino-indan-2-ol. The reaction was found to proceed through a stereoablative process that upgraded the enantioselectivity of an intermediate hydroxy-lactam. The reaction was generally tolerant of a number of substituents in the 4-position, giving enantiomeric excesses of greater than 82%.