82742-16-3

Basic information

• Product Name: .beta.-D-Gulopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-
• Synonyms: .beta.-D-Gulopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-
• CAS NO: 82742-16-3
• Molecular Formula: C₁₃H₁₄O₄
• Molecular Weight: 234.25
• Mol File: 82742-16-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-Gulopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-Gulopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-(82742-16-3)
• EPA Substance Registry System: .beta.-D-Gulopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-(82742-16-3)

Safety Data

• Hazardous Substances Data: 82742-16-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Used in Food Additive Industry:
Due to its sugar-derived nature, .beta.-D-Gulopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)may also find applications in the food additive industry. Its unique structure could potentially be utilized to enhance the taste, texture, or stability of various food products, although further research is needed to explore these possibilities.
Further research and analysis are required to fully understand the potential uses and effects of .beta.-D-Gulopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)in various industries. Its unique structure and properties may offer new opportunities for innovation and development in fields such as pharmaceuticals, food additives, and beyond.

Upstream product

• 34147-05-2 1,6:2,3-dianhydro-β-D-gulopyranose 
• 100-39-0 benzyl bromide 
• 58394-32-4 1,6-anhydro-2,3-dideoxy-β-threo-hex-2-enopyranose 
• 21193-75-9 D-galactal 
• 23643-29-0 1,6-anhydro-4-O-(4-toluenesulfonyl)-β-D-glucopyranose 
• 141054-99-1 1,6-anhydro-4-O-benzyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose 

Downstream Products

• 82742-19-6 1,6-anhydro-4-O-benzyl-3-C-cyano-3-deoxy-β-D-galactopyranose 
• 1353759-07-5 C₁₃H₁₄FN₃O₃ 
• 1353759-06-4 C₁₃H₁₄FN₃O₃ 
• 359772-51-3 1,6-Anhydro-3-azido-4-O-benzyl-3-deoxy-β-D-galactopyranose 
• 82742-20-9 1,6-anhydro-4-O-benzyl-3-C-cyano-3-deoxy-β-D-gulopyranose 
• 359772-53-5 1,6-Anhydro-3-azido-4-O-benzyl-3-deoxy-2-O-tosyl-β-D-galactopyranose 
• 359772-60-4 1,6-anhydro-4-O-benzyl-2,3-dideoxy-2,3-(N-tosylepimino)-β-D-talopyranose 
• 359772-59-1 1,6-Anhydro-4-O-benzyl-2,3-dideoxy-2,3-epimino-β-D-talopyranose 

Relevant articles and documents

Synthesis of fluorinated thiodigalactoside analogues

In this work, we report the first synthesis of fluorinated thiodigalactoside analogues. We used tri-isopropylsilyl thioglycosides as masked glycosyl thiol nucleophiles for the elaboration of two monofluorinated heterodimers, one difluorinated homodimer, and one difluorinated heterodimer. Moreover, we also present an alternative synthesis of 3-deoxy-3-fluorogalactose and 4-deoxy-4-fluorogalactose from a common precursor. Finally, this small set of more stable thiodigalactoside analogues could be interesting inhibitors of galactose-specific lectins.

Reactions of 2-hydroxy-6,8-dioxabicyclo[3.2.1]oct-3-ene with diethylaminosulfur trifluoride and with halogens. Facile synthesis of 1,6- anhydrohalohexopyranoses

D-Galactal 1 reacts in THF in the presence of catalytic amounts of concentrated sulfuric acid to give (2R)-2-hydroxy-6,8-dioxabicyclo[3.2.1]oct- 3-ene (4) in a Ferrier-type rearrangement in 40% yield. When 4 is treated with diethylaminosulfur trifluoride