144728-78-9

Basic information

• Product Name: 3-(dibenzylamino)propyl 2,2,4,4-tetramethyloxazolidine-3-carboxylate
• Synonyms: 3-(dibenzylamino)propyl 2,2,4,4-tetramethyloxazolidine-3-carboxylate
• CAS NO: 144728-78-9
• Molecular Weight: 410.557
• Mol File: 144728-78-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-(dibenzylamino)propyl 2,2,4,4-tetramethyloxazolidine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(dibenzylamino)propyl 2,2,4,4-tetramethyloxazolidine-3-carboxylate(144728-78-9)
• EPA Substance Registry System: 3-(dibenzylamino)propyl 2,2,4,4-tetramethyloxazolidine-3-carboxylate(144728-78-9)

Safety Data

• Hazardous Substances Data: 144728-78-9(Hazardous Substances Data)

Upstream product

• 3161-51-1 3-(N,N-dibenzylamino)-1-propanol 
• 146176-60-5 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carbonyl chloride 
• 57822-91-0 2,2,5,5-tetramethyl-1,3-oxazolidine 

Relevant articles and documents

Enantioselective α-arylation of O-carbamates via sparteine-mediated lithiation and Negishi cross-coupling

A general and highly enantioselective arylation of carbamates derived from primary alcohols was developed by combining Hoppe's sparteine-mediated asymmetric lithiation with Negishi cross-coupling. Coupled with Aggarwal's lithiation-borylation sequence, the current method provides a short and divergent access to a variety of enantioenriched secondary and tertiary benzylic alcohols.