124901-76-4

Basic information

• Product Name: [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate
• Synonyms: [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate
• CAS NO: 124901-76-4
• Molecular Weight: 384.537
• Mol File: 124901-76-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate(124901-76-4)
• EPA Substance Registry System: [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate(124901-76-4)

Safety Data

• Hazardous Substances Data: 124901-76-4(Hazardous Substances Data)

Upstream product

• 74867-37-1 (2R,3R)-1,2,3-Trihydroxydecane 
• 209479-89-0 (4R,5S,4'R)-5-((Z)-Hept-1-enyl)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl] 
• 209479-90-3 (4R,5S,4'R)-5-Heptyl-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl] 
• 13039-94-6 2,3,4,5-di-O-isopropylidene-D-xylose aldehyde 
• 81801-09-4 4-O-benzyl-2,3-O-isopropylidene-D-threose 
• 4762-26-9 hexyltriphenylphosphonium bromide 
• 252188-58-2 (4S,5R)-5-Heptyl-2,2-dimethyl-[1,3]dioxolane-4-carboxylic acid ethyl ester 
• 130967-61-2 [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 124901-75-3 (2R,3R)-1-tosyloxy-2,3-decanediol 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 209479-94-7 (3R,9R,10R)-10-tert-butyldimethylsilyloxy-3-tert-butyldiphenylsilyloxy-heptadec-1-ene-4,6-diyne-9-ol 
• 239473-45-1 (3R,9S,10S)-10-tert-butyldimethylsilyloxy-3-tert-butyldiphenylsilyloxy-heptadec-1-ene-4,6-diyne-9-ol 
• 87005-03-6 (3R,9R,10R)-panaxytriol 
• 128318-02-5 (2S,3S)-1-tosyloxy-2,3-decanediol 
• 124901-75-3 (2R,3R)-1-tosyloxy-2,3-decanediol 

Relevant articles and documents

Synthesis of a new type of antitumour agent panaxytriol: Synthesis of its four diastereomers

Synthesis of four diastereomers of panaxytriol has been described. The basic objective is to create two acetylenic precursors followed by cuprous chloride mediated C-C bond coupling reaction.

First total synthesis of panaxytriol, a potent antitumor agent isolated from Panax ginseng

Panaxytriol 1, a potent antitumor agent isolated from Panax ginseng, was first synthesized, and its stereostructure was confirmed to be (3R, 9R, 10R)-heptadec-1-ene-4,6-diyne-3,9,10-triol.