81562-22-3

Basic information

• Product Name: 1,5-anhydro-3,6-di-O-benzoyl-2-deoxy-4-O-mesyl-D-arabino-hex-1-enitol
• Synonyms: 1,5-anhydro-3,6-di-O-benzoyl-2-deoxy-4-O-mesyl-D-arabino-hex-1-enitol
• CAS NO: 81562-22-3
• Molecular Weight: 432.451
• Mol File: 81562-22-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,5-anhydro-3,6-di-O-benzoyl-2-deoxy-4-O-mesyl-D-arabino-hex-1-enitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-anhydro-3,6-di-O-benzoyl-2-deoxy-4-O-mesyl-D-arabino-hex-1-enitol(81562-22-3)
• EPA Substance Registry System: 1,5-anhydro-3,6-di-O-benzoyl-2-deoxy-4-O-mesyl-D-arabino-hex-1-enitol(81562-22-3)

Safety Data

• Hazardous Substances Data: 81562-22-3(Hazardous Substances Data)

Upstream product

• 13265-84-4 D-glucal 
• 58871-06-0 1,5-anhydro-3,6-di-O-benzoyl-2-deoxy-D-arabino-hex-1-enitol 
• 124-63-0 methanesulfonyl chloride 
• 98-88-4 benzoyl chloride 

Downstream Products

• 475630-51-4 4-azido-4-deoxy-3,6-di-O-benzoyl-D-galactal 
• 1189361-42-9 O-trichloroacetimidoyl {[2,3,4-tri-O-benzyl-β-D-xylopyranosyl-(1->4)]-2,3-di-O-isopropylidene-L-rhamnopyranosyl-(1->2)}-4-azido-4-deoxy-3,6-di-O-benzyl-α-D-galactopyranoside 
• 1392506-69-2 O-triisopropylsilyl {[2,3,4-tri-O-benzyl-β-D-xylopyranosyl-(1->4)]-2,3-di-O-isopropylidene-L-rhamnopyranosyl-(1->2)}-4-azido-4-deoxy-3,6-di-O-benzyl-β-D-galactopyranoside 
• 1189361-01-0 2,6-anhydro-3-azido-1,4-di-O-benzyl-3,5-dideoxy-D-arabino-hex-5-enitol 
• 3971-45-7 methyl 2-deoxy-α-D-galactopyranoside 
• 36396-42-6 Methyl-3,4,6-tri-O-benzoyl-2-desoxy-α-D-lyxo-hexopyranosid 
• 36396-43-7 Methyl-3,4,6-tri-O-benzoyl-2-desoxy-β-D-lyxo-hexopyranosid 
• 475630-54-7 C₂₀H₁₉NO₆ 
• 475630-50-3 4-azido-4-deoxy-3,6-di-O-benzoyl-D-galactal 
• 34948-79-3 1,5-anhydro-3,4,6-tri-O-benzoyl-2-deoxy-D-lyxo-hex-1-enitol 
• 81562-23-4 1,4,6-tri-O-benzoyl-2,3-dideoxy-α-D-threo-hex-2-enopyranose 

Relevant articles and documents

TRITERPENE SAPONIN ANALOGUES

The present application relates to triterpene glycoside saponin-derived adjuvants, syntheses thereof, and intermediates thereto. The application also provides pharmaceutical compositions comprising compounds of the present invention and methods of using said compounds or compositions in the treatment of and immunization for infectious diseases.

TRITERPENE SAPONIN SYNTHESIS, INTERMEDIATES AND ADJUVANT COMBINATIONS

The present application relates to triterpene glycoside saponin-derived adjuvants, syntheses thereof, and intermediates thereto. The application also provides pharmaceutical compositions comprising compounds of the present invention and methods of using said compounds or compositions in the treatment of and immunization for infectious diseases.

Synthesis of γ-aminobutyric acid analogs based on carbohydrate scaffolds

γ-Aminobutyric acid analogs based on sugar scaffolds were prepared in six to nine steps starting from d-glucal and d-galactal. The key step in the synthesis is the Vilsmeier-Haack reaction that affords the corresponding 2-C-formyl glycal on treatment with