440356-62-7

Basic information

• Product Name: 3H,6H-Furo[3,4-c]isoxazol-6-one,tetrahydro-1,4-dimethyl-,(3aR,4S,6aR)-rel-(9CI)
• Synonyms: 3H,6H-Furo[3,4-c]isoxazol-6-one,tetrahydro-1,4-dimethyl-,(3aR,4S,6aR)-rel-(9CI)
• CAS NO: 440356-62-7
• Molecular Formula: C7H11NO3
• Molecular Weight: 157.16714
• Product Categories: GLYCINESCAFFOLD
• Mol File: 440356-62-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3H,6H-Furo[3,4-c]isoxazol-6-one,tetrahydro-1,4-dimethyl-,(3aR,4S,6aR)-rel-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3H,6H-Furo[3,4-c]isoxazol-6-one,tetrahydro-1,4-dimethyl-,(3aR,4S,6aR)-rel-(9CI)(440356-62-7)
• EPA Substance Registry System: 3H,6H-Furo[3,4-c]isoxazol-6-one,tetrahydro-1,4-dimethyl-,(3aR,4S,6aR)-rel-(9CI)(440356-62-7)

Safety Data

• Hazardous Substances Data: 440356-62-7(Hazardous Substances Data)

Upstream product

• 33447-72-2 (R)-3-buten-2-ol 
• 23893-70-1 N-methyl-α-methoxycarbonylmethanimine N-oxide 
• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 440356-57-0 1-methylprop-2-enyl hydroxy[(1-methylprop-2-enyl)-oxy]acetate 
• 598-32-3 2-hydroxy-3-butene 

Relevant articles and documents

Intramolecular cycloadditions of α-allyloxycarbonylnitrones: Stereoselective synthesis of 3-amino-2(5h)furanones

Treatment offuroisoxazolidines with NaH leads to functionalized 3-amino-2(5H)-furanones through a new rearrangement pattern of the isoxazolidine nucleus. This process has been usefully exploited for the synthesis of enantiomerically pure (5R)-3-alkylamino