929296-60-6

Basic information

• Product Name: C₃₈H₆₀O₁₀
• Synonyms: C₃₈H₆₀O₁₀
• CAS NO: 929296-60-6
• Molecular Weight: 676.888
• Mol File: 929296-60-6.mol

Chemical Properties

• CAS DataBase Reference: C₃₈H₆₀O₁₀(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₈H₆₀O₁₀(929296-60-6)
• EPA Substance Registry System: C₃₈H₆₀O₁₀(929296-60-6)

Safety Data

• Hazardous Substances Data: 929296-60-6(Hazardous Substances Data)

Upstream product

• 182818-70-8 1-(methoxycarbonyl)pentadec-10(S)-yl α-L-rhamnopyranoside 
• 1513847-21-6 1-(methoxycarbonyl)pentadec-10(S)-yl 2,3-didehydro-4-O-benzyl-α-L-rhamnopyranosyl-(1→4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 1513847-22-7 1-(methoxycarbonyl)pentadec-10(S)-yl 4-O-benzyl-α-L-rhamnopyranosyl-(1→4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 1513847-18-1 1-(methoxycarbonyl)pentadec-10(S)-yl 2,3-didehydro-α-L-rhamnopyranoside 
• 1513847-17-0 C₂₃H₄₀O₅ 
• 13717-17-4 (S)-11-hydroxyhexadecanoic acid 
• 121043-05-8 (S)-methyl 11-hydroxyhexadecanoate 
• 180782-40-5 (12S)-12-[(tert-butyldimethylsilyl)oxy]-1-heptadecyne 
• 66-25-1 hexanal 
• 2243-98-3 1-undecyne 
• 180782-37-0 (12S)-12-hydroxy-1-heptadecyne 
• 197853-44-4 11(S)-acetoxy-1-hexadecanoic acid 
• 929296-54-8 (S)-11-((2R,3R,4R,5S,6S)-3,4,5-Triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexadecanoic acid methyl ester 
• 115655-84-0 1-(methoxycarbonyl)pentadec-10(S)-yl 2,3-O-isopropylidene-α-L-rhamnopyranoside 

Relevant articles and documents

Merremoside D: De novo synthesis of the purported structure, nmr analysis, and comparison of spectral data

The first synthesis of the purported structure of Merremoside D has been achieved in 22 longest linear steps. The de novo asymmetric synthesis relied on the use of asymmetric catalysis to selectively install all 21 stereocenters in the final compounds fro

Syntheses of the macrolide subunits of merremoside-type resin glycosides

The 20- and 21-membered macrolide subunits of merremoside-type resin glycosides with interesting bioactivity were synthesized via a macrolactonization approach using Corey-Nicolaou protocol in 14 steps with overall yields of 0.7% for 17 and 3.5% for 18 fr