32453-58-0

Basic information

• Product Name: methyl-2,3,4-tri-O-acetyl-6-deoxy-β-L-glucopyranoside
• Synonyms: methyl-2,3,4-tri-O-acetyl-6-deoxy-β-L-glucopyranoside
• CAS NO: 32453-58-0
• Molecular Weight: 290.27
• Mol File: 32453-58-0.mol

Chemical Properties

• CAS DataBase Reference: methyl-2,3,4-tri-O-acetyl-6-deoxy-β-L-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl-2,3,4-tri-O-acetyl-6-deoxy-β-L-glucopyranoside(32453-58-0)
• EPA Substance Registry System: methyl-2,3,4-tri-O-acetyl-6-deoxy-β-L-glucopyranoside(32453-58-0)

Safety Data

• Hazardous Substances Data: 32453-58-0(Hazardous Substances Data)

Upstream product

• 91-09-8 methyl α-L-xylopyranoside 
• 108-24-7 acetic anhydride 
• 95851-48-2 C₄₂H₆₈O₁₂ 
• 91-09-8 methyl α,β-L-xyloside 
• 67-56-1 methanol 
• 4049-33-6 tetra-O-acetyl-β-D-xylopyranose 
• 19186-38-0 O¹,O³,O⁴-Triacetyl-α-D-xylopyranose 
• 74-88-4 methyl iodide 
• 612-05-5 methyl-β-D-xylopyranoside 
• 32453-59-1 (2R,3S,4R,5R)-2-methoxytetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 532-20-7 D-arabinofuranose 
• 53448-52-5 methyl β-L-xylopyranoside 

Downstream Products

• 34168-73-5 1,2,3,4,5-penta-O-acetyl-aldehydo-D-arabinose, methyl semiacetal 
• 32453-59-1 (2R,3S,4R,5R)-2-methoxytetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 19186-37-9 1,2,3,4-tetra-O-acetyl-α-D-arabinopyranose 
• 25243-38-3 1,2,3,4-tetra-O-acetyl-β-D-arabinopyranose 
• 13035-61-5 1,2,3,5-tetra-O-acetyl-α-D-arabinofuranose 
• 13035-61-5 1,2,3,5-tetra-O-acetyl-β-D-arabinofuranose 
• 612-05-5 methyl-β-D-xylopyranoside 
• 74162-08-6 methyl 2,4-di-O-acetyl-β-D-xylopyranoside 
• 41897-35-2 methyl 2-mono-O-acetyl-β-D-xylopyranoside 
• 77217-82-4 methyl 3,4-di-O-acetyl-β-D-xylopyranoside 

Relevant articles and documents

ACTIVE AGENTS AND METHODS OF THEIR USE FOR THE TREATMENT OF METABOLIC DISORDERS AND NONALCOHOLIC FATTY LIVER DISEASE

Disclosed herein are active agents, compositions containing them, unit dosage forms containing them, and methods of their use, e.g., for treating a metabolic disorder or nonalcoholic fatty liver disease or for modulating a metabolic marker or nonalcoholic fatty liver disease marker.

Synthesis of C7-C16-alkyl glycosides: Part II - Synthesis of alkyl d-xylopyranosides in the presence of tin(IV) chloride as a Lewis acid catalyst

The Lewis acid catalyzed glycosylation reaction of β-peracetylated sugar derivatives (xylose) with fatty alkanols is used in a synthesis of C7-C16-alkyl D-xylopyranosides. The process occurs under the influence of tin(IV) chloride.

Synthesis of acylated methyl β-D-xylopyranosides and their enzymic deacylations by rabbit serum esterases

Selective pivaloylations of methyl β-D-xylopyranoside have been studied under various reaction conditions. Partially pivaloylated products were submitted to additional acetylations. The structures were established by 1H NMR spectroscopy. Representatives of acylated methyl β-D-xylopyranosides (acyl being pivaloyl, acetyl, or a combination of both) were submitted to hydrolysis catalyzed by rabbit serum and esterases isolated from rabbit serum.

Oviposition Deterrent of a Rutaceae-feeding Swallowtail Butterfly, Papilio xuthus, from a Non-host Rutaceous Plant, Orixa japonica

Females of the Rutaceae-feeding swallowtail butterfly, Papilio xuthus, do not oviposit on the rutaceous plant, Orixa japonica.A methanolic extract of O. japonica leaves was found to contain contact-chemical factors which deterred oviposition of the butter