124901-75-3

Basic information

• Product Name: (2R,3R)-1-tosyloxy-2,3-decanediol
• Synonyms: (2R,3R)-1-tosyloxy-2,3-decanediol
• CAS NO: 124901-75-3
• Molecular Weight: 344.472
• Mol File: 124901-75-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (2R,3R)-1-tosyloxy-2,3-decanediol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-1-tosyloxy-2,3-decanediol(124901-75-3)
• EPA Substance Registry System: (2R,3R)-1-tosyloxy-2,3-decanediol(124901-75-3)

Safety Data

• Hazardous Substances Data: 124901-75-3(Hazardous Substances Data)

Upstream product

• 124901-76-4 [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate 
• 123932-68-3 (2R,3S)-3-heptyloxirane methanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 21369-64-2 n-hexyllithium 
• 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] 
• 220125-71-3 [(4S,5S)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methanol 
• 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 
• 245068-66-0 [(4S,5S)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate 
• 74867-37-1 (2R,3R)-1,2,3-Trihydroxydecane 

Downstream Products

• 124901-76-4 [(4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl]methyl 4-methyl-1-benzenesulfonate 
• 87005-03-6 (3R,9R,10R)-panaxytriol 
• 130258-88-7 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (S)-1-ethyl-6-((4R,5R)-5-heptyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexa-2,4-diynyl ester 
• 130258-88-7 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-1-ethyl-6-((4R,5R)-5-heptyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexa-2,4-diynyl ester 
• 209479-94-7 (3R,9R,10R)-10-tert-butyldimethylsilyloxy-3-tert-butyldiphenylsilyloxy-heptadec-1-ene-4,6-diyne-9-ol 

Relevant articles and documents

Synthesis of panaxytriol and its stereoisomers as potential antitumor drugs

An efficient synthesis of panaxytriol and its seven stereoisomers was achieved, and four unnatural diastereomers of 2a were prepared. The key steps involved the opening of vicinal hydroxy epoxides, the stereospecific opening of the epoxides with perchlori

Syntheses of two diastereoisomers of panaxytriol, a potent antitumor agent isolated from Panax ginseng

(3R, 9R, 10R) and (3R, 9S, 10S) diastereoisomers (2 and 3) of panaxytriol (1) were synthesized, and the absolute configuration of panaxytriol was confirmed as (3R, 9R, 10R)-heptadec-1-ene-4,6-diyne-3,9,10- triol.

Synthesis and absolute configurations of the cytotoxic polyacetylenes isolated from the callus of Panax ginseng

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