6386-26-1

Basic information

• Product Name: O¹,O²-isopropylidene-O⁵-benzyl-α-D-glucofuranose
• CAS NO: 6386-26-1
• Molecular Weight: 310.347
• Mol File: 6386-26-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: O¹,O²-isopropylidene-O⁵-benzyl-α-D-glucofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: O¹,O²-isopropylidene-O⁵-benzyl-α-D-glucofuranose(6386-26-1)
• EPA Substance Registry System: O¹,O²-isopropylidene-O⁵-benzyl-α-D-glucofuranose(6386-26-1)

Safety Data

• Hazardous Substances Data: 6386-26-1(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 
• 3067-56-9 D-glucurono-3,6-lactone acetonide 
• 14362-29-9 α-D-glucurono-γ-lactone 
• 5111-13-7 (1S,3R,4R,5S,8S)-8-benzyloxy-7-keto-3,4-isopropylidenedioxy-2,6-dioxabicyclo[3.3.0]octane 

Downstream Products

• 5123-94-4 5-Benzyl-D-glucofuranose 
• 849624-17-5 (1S,4S,5R,8R)-4-acetamido-8-benzyloxy-3-(tert-butyldimethylsilyloxy)-2,6-dioxabicyclo[3.3.0]octane 
• 849624-14-2 (1R,4R,5R,8R)-8-benzyloxy-3-methoxy-4-hydroxy-2,6-dioxabicyclo[3.3.0]octane 
• 849624-15-3 (1S,4S,5R,8R)-4-azido-8-benzyloxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane 
• 849624-16-4 (1S,4S,5R,8R)-4-acetamido-8-benzyloxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane 
• 142719-12-8 C₂₂H₃₆O₆Si 
• 1394245-90-9 C₃₉H₇₂O₉Si₄ 
• 864512-90-3 trans-caffeoyl-6-O-D-glucono-γ-lactone 
• 1394245-97-6 C₂₅H₃₂O₇ 
• 1394245-92-1 C₂₀H₂₂O₆ 
• 1394245-94-3 C₃₉H₇₂O₉Si₄ 
• 1394245-99-8 (5S)-epi-vittarilide A 
• 1394245-86-3 C₂₄H₄₀O₇Si 
• 5123-95-5 5-Benzyl-D-glucose-phenylosazon 

Relevant articles and documents

First total synthesis and absolute stereochemical assignment of vittarilide-A, an antioxidant extractive component isolated from Vittaria anguste-elongata Hayata

The first stereocontrolled synthesis of vittarilide-A and its C5-epimer was completed from d-glucuronolactone. Comparison with the spectroscopic properties reported for authentic material has given a clear indication as to the absolute stereochemistry of the natural vittarilide-A.

An efficient and straightforward synthetic process to an amino sugar analogue, furanodictine B

A convenient and practical strategy for the construction of a natural amino sugar analogue, furanodictine B, isolated from the multicellular fruit body has been developed in an optically active form. The synthetic process is based on readily accessible and stereodefmed manipulation of the highly functionalized bicyclic derivative incorporating the glucuronolactone-derived skeleton.