143724-93-0

Basic information

• Product Name: (S)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-ynoic acid methyl ester
• CAS NO: 143724-93-0
• Molecular Weight: 340.443
• Mol File: 143724-93-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-ynoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-ynoic acid methyl ester(143724-93-0)
• EPA Substance Registry System: (S)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-ynoic acid methyl ester(143724-93-0)

Safety Data

• Hazardous Substances Data: 143724-93-0(Hazardous Substances Data)

Upstream product

• 143724-91-8 (S)-1-Phenyl-1-phenylsulfanyl-6-trimethylsilanyl-hex-5-yn-3-ol 
• 148516-14-7 (S)-2-(3-trimethylsilyl-2-propynyl)oxirane 
• 148516-13-6 (S)-1-chloro-2-hydroxy-5-trimethylsilyl-4-pentyne 
• 831-91-4 Benzyl phenyl sulfide 
• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 143724-92-9 (S)-1-Phenyl-1-phenylsulfanyl-hex-5-yn-3-ol 
• 143724-91-8 (R)-1-Phenyl-1-phenylsulfanyl-6-trimethylsilanyl-hex-5-yn-3-ol 
• 143724-89-4 Trimethyl-((R)-3-oxiranyl-prop-1-ynyl)-silane 
• 143724-90-7 (2R)-1-chloro-5-(trimethylsilyl)pent-4-yn-2-ol 
• 143724-92-9 (R)-1-Phenyl-1-phenylsulfanyl-hex-5-yn-3-ol 

Downstream Products

• 22639-28-7 (R)-goniothalamin 
• 143724-95-2 (R)-6-(2-Phenyl-2-phenylsulfanyl-ethyl)-5,6-dihydro-pyran-2-one 
• 143724-96-3 (R)-6-(2-Benzenesulfinyl-2-phenyl-ethyl)-5,6-dihydro-pyran-2-one 
• 122046-62-2 (S)-goniothalamin 
• 143724-97-4 (1R,4S,6R)-4-((E)-Styryl)-3,7-dioxa-bicyclo[4.1.0]heptan-2-one 
• 143724-95-2 (S)-6-(2-Phenyl-2-phenylsulfanyl-ethyl)-5,6-dihydro-pyran-2-one 
• 143724-96-3 (S)-6-(2-Benzenesulfinyl-2-phenyl-ethyl)-5,6-dihydro-pyran-2-one 
• 143724-94-1 (Z)-(S)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-enoic acid methyl ester 
• 143724-94-1 (Z)-(R)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-enoic acid methyl ester 

Relevant articles and documents

Stereocontrolled Route to the δ-Benzylidenemethyl-β-hydroxy-δ-lactone System Utilizing a New Chiral Epoxyacetylene Building Block

Stereocontrolled route to the δ-benzylidenemethyl-β-hydroxy-δ-lactone system has been developed utilizing a new epoxyacetylene building block prepared from optically active epichlorohydrin.The present synthesis allowed efficient construction of goniothalamin in natural and unnatural forms and its 3-hydroxy derivative having the essential anti-β/δ-stereochemistry for HMG Co-A reductase inhibition.