119116-61-9

Basic information

• Product Name: O-benzyl-enantio-ineupatoriol
• CAS NO: 119116-61-9
• Molecular Weight: 338.47
• Mol File: 119116-61-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: O-benzyl-enantio-ineupatoriol(CAS DataBase Reference)
• NIST Chemistry Reference: O-benzyl-enantio-ineupatoriol(119116-61-9)
• EPA Substance Registry System: O-benzyl-enantio-ineupatoriol(119116-61-9)

Safety Data

• Hazardous Substances Data: 119116-61-9(Hazardous Substances Data)

Upstream product

• 119116-55-1 O-(1,5-anhydro-2-deoxy-4,6-O-benzylidene-D-ribohexityl) S-methyl dithiocarbonate 
• 119116-56-2 (2R,3S)-<3-(benzyloxy)tetrahydropyran-2-yl>methanol 
• 63598-39-0 (2R,4aR,8aS)-2-phenylhexahydropyrano<3,2-d>-1,3-dioxin 
• 501-91-7 junipal 
• 119116-57-3 (2R,3S)-3-(benzyloxy)tetrahydropyran-2-carbaldehyde 
• 119116-60-8 (5-propynyl-2-thienyl)triphenylphosphonium chloride 
• 119116-59-5 2-(chloromethyl)-5-(prop-1-ynyl)thiophene 
• 119116-58-4 5-(prop-1-ynyl)-2-thiophenemethanol 
• 119238-15-2 1,5-anhydro-2-deoxy-4,6-O-benzylidene-D-ribohexitol 

Relevant articles and documents

A CONVERGENT SYNTHESIS OF THE O-BENZYL DERIVATIVE OF ENANTIO-INEUPATORIOL FROM A CARBOHYDRATE PRECURSOR

The trans-2,3-disubstituted tetrahydropyran 7, obtained in eight steps from methyl α-D-glucoside, and the phosphonium salt 10, obtained from thiophene in six steps, were successfully combined in a Wittig reaction to form 11, the O-benzyl enantiomer of the