109959-17-3

Basic information

• Product Name: 4-((1S,4R,5S,6S)-4,5,6-Tris-benzyloxy-3-trityloxymethyl-cyclohex-2-enyloxy)-benzo[d][1,2]oxazin-1-one
• CAS NO: 109959-17-3
• Molecular Weight: 833.981
• Mol File: 109959-17-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-((1S,4R,5S,6S)-4,5,6-Tris-benzyloxy-3-trityloxymethyl-cyclohex-2-enyloxy)-benzo[d][1,2]oxazin-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((1S,4R,5S,6S)-4,5,6-Tris-benzyloxy-3-trityloxymethyl-cyclohex-2-enyloxy)-benzo[d][1,2]oxazin-1-one(109959-17-3)
• EPA Substance Registry System: 4-((1S,4R,5S,6S)-4,5,6-Tris-benzyloxy-3-trityloxymethyl-cyclohex-2-enyloxy)-benzo[d][1,2]oxazin-1-one(109959-17-3)

Safety Data

• Hazardous Substances Data: 109959-17-3(Hazardous Substances Data)

Upstream product

• 109959-12-8 (1R,2S,3S,4R)-2,3,4-tri-O-benzyl-5-(trityloxymethyl)-5-cyclohexene-1,2,3,4-tetrol 
• 31583-39-8 3H-benzo[d][1,2]oxazine-1,4-dione 
• 76-83-5 trityl chloride 
• 85716-47-8 (1R,2R,3S,4R)-1,2,3-tri-O-benzyl-6-bromo-4-(bromomethyl)-4-cyclohexene-1,2,3-triol 
• 75348-19-5 1L-(1,2/2,4)-2,3,4-Tri-O-benzyl-5-C-(hydroxymethyl)-5-cyclohexen-1,2,3,4-tetrol 
• 105017-77-4 1D-(1,2,4/3)-2,3,4-Tri-O-benzyl-5-C-(hydroxymethyl)-5-cyclohexen-1,2,3,4-tetrol 
• 109923-16-2 (1S,2S,3S,4R)-2,3,4-tri-O-benzyl-5-(trityloxymethyl)-5-cyclohexene-1,2,3,4-tetrol 
• 109923-15-1 (1S,2S,3S,4R)-1-O-benzoyl-5-(benzoyloxymethyl)-2,3,4-tri-O-benzyl-5-cyclohexene-1,2,3,4-tetrol 
• 109923-15-1 (1R,2S,3S,4R)-1-O-benzoyl-5-(benzoyloxymethyl)-2,3,4-tri-O-benzyl-5-cyclohexene-1,2,3,4-tetrol 
• 109923-17-3 (1R,2S,3S,4R)-1-O-benzoyl-2,3,4-tri-O-benzyl-5-(trityloxymethyl)-5-cyclohexene-1,2,3,4-tetrol 
• 109923-17-3 (1S,2S,3S,4R)-1-O-benzoyl-2,3,4-tri-O-benzyl-5-(trityloxymethyl)-5-cyclohexene-1,2,3,4-tetrol 

Relevant articles and documents

DISPLACEMENT OF "PSEUDOANOMERIC" HYDROXYL GROUPS BY USING THE DIETHYL AZODICARBOXYLATE-TRIPHENYLPHOSPHINE SYSTEM

1D-(1,2,4/3)-2,3,4-Tri-O-benzyl-5-(trityloxymethyl)-5-cyclohexene-1,2,3,4-tetrol (5a) and its 1L-(1,3/2,4) isomer (5b) were prepared from D-glucose, and they underwent ready mutual interconversion through an SN2 procedure employing a benzoic ac