1198616-15-7

Basic information

• Product Name: (2R,4S)-1-acetoxy-2,4-O-isopropylidene-1-(p-tolylsulfanyl)-5-(triphenylmethyloxy)pentane-2,4-diol
• Synonyms: (2R,4S)-1-acetoxy-2,4-O-isopropylidene-1-(p-tolylsulfanyl)-5-(triphenylmethyloxy)pentane-2,4-diol
• CAS NO: 1198616-15-7
• Molecular Weight: 582.761
• Mol File: 1198616-15-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,4S)-1-acetoxy-2,4-O-isopropylidene-1-(p-tolylsulfanyl)-5-(triphenylmethyloxy)pentane-2,4-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,4S)-1-acetoxy-2,4-O-isopropylidene-1-(p-tolylsulfanyl)-5-(triphenylmethyloxy)pentane-2,4-diol(1198616-15-7)
• EPA Substance Registry System: (2R,4S)-1-acetoxy-2,4-O-isopropylidene-1-(p-tolylsulfanyl)-5-(triphenylmethyloxy)pentane-2,4-diol(1198616-15-7)

Safety Data

• Hazardous Substances Data: 1198616-15-7(Hazardous Substances Data)

Upstream product

• 1198616-14-6 (S(R),2R,4S)-2,4-O-isopropylidene-1-(p-tolylsulfinyl)-5-(triphenylmethyloxy)pentane-2,4-diol 
• 108-24-7 acetic anhydride 

Downstream Products

• 1198616-16-8 (2R,4S)-2,4-O-isopropylidene-5-(triphenylmethyloxy)pentane-1,2,4-triol 

Relevant articles and documents

Structure elucidation and stereoselective total synthesis of pavettamine, the causal agent of gousiekte

The structure elucidation of a novel natural product pavettamine (1), the causal agent of the plant toxicosis gousiekte, is reported. The structure was defined by analysis of NMR and MS data and the relative configuration followed from the 13C NMR data of the acetonide derivative. The absolute stereochemistry was established by total synthesis from (2S)-malic acid using chiral sulfoxide methodology as (2S,4R,8R,10S)-1,11-diamino-6-aza-undecane-2,4,8,10-tetraol.