1268616-18-7

Basic information

• Product Name: (2S,3R,4R)-3-(benzyloxy)-4-(methoxymethoxy)hept-6-ene-1,2-diol
• Synonyms: (2S,3R,4R)-3-(benzyloxy)-4-(methoxymethoxy)hept-6-ene-1,2-diol
• CAS NO: 1268616-18-7
• Molecular Weight: 296.364
• Mol File: 1268616-18-7.mol

Chemical Properties

• CAS DataBase Reference: (2S,3R,4R)-3-(benzyloxy)-4-(methoxymethoxy)hept-6-ene-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4R)-3-(benzyloxy)-4-(methoxymethoxy)hept-6-ene-1,2-diol(1268616-18-7)
• EPA Substance Registry System: (2S,3R,4R)-3-(benzyloxy)-4-(methoxymethoxy)hept-6-ene-1,2-diol(1268616-18-7)

Safety Data

• Hazardous Substances Data: 1268616-18-7(Hazardous Substances Data)

Upstream product

• 1268616-25-6 C₁₉H₂₈O₅ 
• 84379-53-3 2-O-benzyl-3,4-O-isopropylidene-L-threitol 
• 100906-42-1 2-O-benzyl-3,4-O-isopropylidene-L-threose 
• 111462-27-2 (1S,2R)-1-(benzyloxy)-1-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)pent-4-en-2-ol 

Downstream Products

• 1268616-19-8 (2S,3R,4R)-3-(benzyloxy)-1-(tert-butyldimethylsilyloxy)-4-(methoxymethoxy)-2-(p-toluenesulfonyloxy)-hept-6-ene 
• 1268616-26-7 C₂₂H₃₈O₅Si 
• 1340476-25-6 (3S,4S,5R)-5-allyl-4-(benzyloxy)tetrahydrofuran-3-yl 4-methylbenzenesulfonate 
• 1340476-26-7 (3R,4R,5R)-5-allyl-N-benzyl-4-(benzyloxy)tetrahydrofuran-3-amine 
• 1340476-27-8 (3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine 
• 1340476-24-5 (2S,3R,4R)-3-(benzyloxy)-2-hydroxy-4-(methoxymethoxy)hept-6-enyl 4-methylbenzenesulfonate 
• 1312103-69-7 (3aS,8R,11aS,Z)-8-((R)-1-(benzyloxy)heptyl)-2,2-dimethyl-4,5,8,9-tetrahydro-3aH-[1,3]dioxolo[4,5-e]oxecin-6(11aH)-one 
• 1312103-58-4 (3aS,8R,11aS,E)-8-((R)-1-(benzyloxy)heptyl)-2,2-dimethyl-4,5,8,9-tetrahydro-3aH-[1,3]dioxolo[4,5-e]oxecin-6(11aH)-one 
• 1312103-59-5 (4R,5R)-5-(benzyloxy)undec-1-en-4-yl 3-((4S,5S)-2,2-dimethyl-5-vinyl-1,3-dioxolan-4-yl)propanoate 
• 1312103-68-6 (4S,5S)-5-(benzyloxy)undec-1-en-4-ol 
• 1312103-62-0 ((((4R,5R)-4-(methoxymethoxy)undec-1-en-5-yl)oxy)methyl)benzene 
• 1312103-61-9 (2R,3R)-2-(enzyloxy)-3-(methoxymethoxy)hex-5-en-1-ol 

Relevant articles and documents

Stereoselective total synthesis of (+)-synargentolide A

The stereoselective synthesis of synargentolide A, a polyhydroxy δ-lactone, has been accomplished from tartaric acid. The key steps in the synthesis involve Keck and Brown allylations and ring closing metathesis.

Total synthesis of (-)-ent-pachastrissamine (ent-Jaspine B)

The total synthesis of the enantiomer of the tetrahydrofuran containing natural product Jaspine B is reported. The key reactions in the synthesis include formation of the tetrahydrofuran unit by an acid mediated Williamson etherification and a subsequent