148028-26-6

Basic information

• Product Name: 2-Oxazolidinone,4-(1-methylethyl)-3-(2-propenyl)-,(S)-(9CI)
• Synonyms: 2-Oxazolidinone,4-(1-methylethyl)-3-(2-propenyl)-,(S)-(9CI)
• CAS NO: 148028-26-6
• Molecular Formula: C9H15NO2
• Molecular Weight: 169.22
• Product Categories: ISOPROPYL
• Mol File: 148028-26-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Oxazolidinone,4-(1-methylethyl)-3-(2-propenyl)-,(S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone,4-(1-methylethyl)-3-(2-propenyl)-,(S)-(9CI)(148028-26-6)
• EPA Substance Registry System: 2-Oxazolidinone,4-(1-methylethyl)-3-(2-propenyl)-,(S)-(9CI)(148028-26-6)

Safety Data

• Hazardous Substances Data: 148028-26-6(Hazardous Substances Data)

Upstream product

• 79069-14-0 (S)-2-<(tert-butoxycarbonyl)amino>-3-methylbutan-1-ol 
• 106-95-6 allyl bromide 
• 6216-65-5 N-benzyloxycarbonyl-L-valinol 
• 17016-83-0 (4S)-4-isopropyl-1,3-oxazolidin-2-one 

Relevant articles and documents

One Pot Synthesis of N-Derivatized 2-Oxazolidinones from Amino Alcohol Carbamates

A one pot protocol for the synthesis of N-derivatized 2-oxazolidinones from amino alcohol carbamates is described.The method is exceptionally useful if the parent amino acids are prepared in their enantiopure forms via enzymatic resolution of the racemic carbamate esters.

Conjugate addition of organocuprates to methyl crotonate linked to chiral oxazolidones

Conjugate addition of various sp3 dialkylcuprates were performed on enoates 4a-b, γ-aminocrotonate equivalents embodied in chiral oxazolidones. The diastereoselectivity is good to moderate and allows the access to homochiral β-substituted GABA analogues.