1427201-87-3

Basic information

• Product Name: C₅₃H₆₀O₇
• Synonyms: C₅₃H₆₀O₇
• CAS NO: 1427201-87-3
• Molecular Weight: 809.055
• Mol File: 1427201-87-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₅₃H₆₀O₇(CAS DataBase Reference)
• NIST Chemistry Reference: C₅₃H₆₀O₇(1427201-87-3)
• EPA Substance Registry System: C₅₃H₆₀O₇(1427201-87-3)

Safety Data

• Hazardous Substances Data: 1427201-87-3(Hazardous Substances Data)

Upstream product

• 1427201-63-5 (2R,6S)-2-((benzyloxy)methyl)-6-(octyloxy)-2H-pyran-3(6H)-one 
• 1427201-60-2 (2R,6R)-6-((benzyloxy)methyl)-5-oxo-5,6-dihydro-2H-pyran-2-yl tert-butyl carbonate 
• 76-84-6 triphenylmethyl alcohol 
• 63802-97-1 (R)-1-(2-furyl)-2-O-benzyl-1,2-ethanediol 
• 1427201-65-7 (2R,3S,6S)-2-((benzyloxy)methyl)-6-(((2R,3S,6S)-2-((benzyloxy)methyl)-6-(octyloxy)-3,6-dihydro-2H-pyran-3-yl)-oxy)-3,6-dihydro-2H-pyran-3-ol 
• 115726-23-3 triphenylmethyl trifluoromethanesulfonate 
• 1427201-64-6 (2R,3S,6S)-2-((benzyloxy)methyl)-6-(octyloxy)-3,6-dihydro-2H-pyran-3-ol 
• 111-87-5 octanol 

Relevant articles and documents

Regioselective polymethylation of α-(1 → 4)-linked mannopyranose oligosaccharides

An approach has been developed of the regioselective methylation of α-(1 → 4)-linked mannopyranose oligosaccharides via a four-step methodology. The key reaction involved n-Bu2SnCl2-mediated activation of cis-diols. By tuning protecting groups on the substrates, multiple cis-diols in the substrates were functionalized in a consistent and regioselective manner. Using optimized substrates and reaction conditions, regioselective methylation of di-, tri-, and tetrasaccharide substrates proceeded in isolated yields per cis-diol of 95, 88 and 79%, respectively. The methodology was also applied to functionalize trans-diols in α-cyclodextrin.