1268624-99-2

Basic information

• Product Name: 4-methoxybenzyl 2,3-anhydro-6-deoxy-α-D-allopyranoside
• Synonyms: 4-methoxybenzyl 2,3-anhydro-6-deoxy-α-D-allopyranoside
• CAS NO: 1268624-99-2
• Molecular Weight: 266.294
• Mol File: 1268624-99-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-methoxybenzyl 2,3-anhydro-6-deoxy-α-D-allopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxybenzyl 2,3-anhydro-6-deoxy-α-D-allopyranoside(1268624-99-2)
• EPA Substance Registry System: 4-methoxybenzyl 2,3-anhydro-6-deoxy-α-D-allopyranoside(1268624-99-2)

Safety Data

• Hazardous Substances Data: 1268624-99-2(Hazardous Substances Data)

Upstream product

• 27948-61-4 (R)-(+)-1-(2-furyl)ethanol 
• 1192-62-7 1-(2-furyl)-1-ethanone 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 1268625-01-9 C₂₀H₃₃N₃O₅Si 
• 1268625-02-0 C₂₂H₃₅N₃O₆Si 
• 1268625-00-8 C₂₀H₃₂O₅Si 
• 1440917-68-9 C₂₁H₃₆O₇SSi 
• 1440917-73-6 C₂₀H₃₃N₃O₄Si 
• 1440917-04-3 C₂₀H₃₄O₅Si 
• 1440917-62-3 C₂₀H₃₂O₅Si 

Relevant articles and documents

Total Synthesis and Biological Evaluation of the Glycosylated Macrocyclic Antibiotic Mangrolide A

The macrocyclic antibiotic mangrolide A has been described to exhibit potent activity against a number of clinically important Gram-negative pathogens. Reported is the first enantioselective total synthesis of mangrolide A and derivatives. Salient features of this synthesis include a highly convergent macrocycle preparation, stereoselective synthesis of the disaccharide moiety, and two β-selective glycosylations. The synthesis of mangrolide A and its analogues enabled the re-examination of its activity against bacterial pathogens, and only minimal activity was observed.