127566-14-7

Basic information

• Product Name: (1S,2R)-(-)-2-(N,N-di-n-pentylamino)-1-phenylpropan-1-ol
• Synonyms: (1S,2R)-(-)-2-(N,N-di-n-pentylamino)-1-phenylpropan-1-ol
• CAS NO: 127566-14-7
• Molecular Weight: 291.477
• Mol File: 127566-14-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2R)-(-)-2-(N,N-di-n-pentylamino)-1-phenylpropan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R)-(-)-2-(N,N-di-n-pentylamino)-1-phenylpropan-1-ol(127566-14-7)
• EPA Substance Registry System: (1S,2R)-(-)-2-(N,N-di-n-pentylamino)-1-phenylpropan-1-ol(127566-14-7)

Safety Data

• Hazardous Substances Data: 127566-14-7(Hazardous Substances Data)

Upstream product

• 628-17-1 amyl iodide 
• 37577-28-9 (1S,2R)-(+)-norphedrine 

Relevant articles and documents

Chiral N,N-Dialkylnorephedrines as Catalysts of the Highly Enantioselective Addition of Dialkylzincs to Aliphatic and Aromatic Aldehydes. The Asymmetric Synthesis of Secondary Aliphatic and Aromatic Alcohols of High Optical Purity

The chiral N,N-dialkylnorephedrine-catalyzed addition of dialkylzincs to aliphatic and aromatic aldehydes afforded secondary alcohols of high optical purity (to > 95percent ee).Among the N,N-di(primary alkyl)norephedrines, N,N-di-n-butylnorephedrine (DBNE, 3d) was found to be the most effective catalyst. 1-Phenyl-2-(1-pyrrolidinyl)propan-1-ol (3i) and N,N-diallylnorephedrine (3j) were also highly effective catalysts.The method described provides optically active secondary aliphatic alcohols of high optical purity which cannot be prepared by conventional methods.