143724-96-3

Basic information

• Product Name: 2H-Pyran-2-one, 5,6-dihydro-6-[2-phenyl-2-(phenylsulfinyl)ethyl]-
• CAS NO: 143724-96-3
• Molecular Formula: C19H18O3S
• Molecular Weight: 326.416
• Mol File: 143724-96-3.mol

Chemical Properties

• CAS DataBase Reference: 2H-Pyran-2-one, 5,6-dihydro-6-[2-phenyl-2-(phenylsulfinyl)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran-2-one, 5,6-dihydro-6-[2-phenyl-2-(phenylsulfinyl)ethyl]-(143724-96-3)
• EPA Substance Registry System: 2H-Pyran-2-one, 5,6-dihydro-6-[2-phenyl-2-(phenylsulfinyl)ethyl]-(143724-96-3)

Safety Data

• Hazardous Substances Data: 143724-96-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2H-Pyran-2-one, 5,6-dihydro-6-[2-phenyl-2-(phenylsulfinyl)ethyl]is used as a potential pharmaceutical agent for its unique chemical structure and properties. Its specific application reason in this industry is due to its potential to interact with biological targets and exhibit therapeutic effects, which can be further explored through research and development.
Used in Agrochemical Industry:
In the agrochemical industry, 2H-Pyran-2-one, 5,6-dihydro-6-[2-phenyl-2-(phenylsulfinyl)ethyl]is used as a potential active ingredient in the development of new pesticides or herbicides. Its application reason lies in its unique chemical properties that may provide novel modes of action or enhanced efficacy in controlling pests and weeds.
Used in Materials Science:
2H-Pyran-2-one, 5,6-dihydro-6-[2-phenyl-2-(phenylsulfinyl)ethyl]is utilized in materials science as a component in the development of new materials with specific properties. Its application reason is attributed to its unique chemical structure, which may contribute to the creation of materials with improved performance characteristics, such as enhanced stability, reactivity, or selectivity in various applications.

Upstream product

• 143724-95-2 (S)-6-(2-Phenyl-2-phenylsulfanyl-ethyl)-5,6-dihydro-pyran-2-one 
• 831-91-4 Benzyl phenyl sulfide 
• 148516-13-6 (S)-1-chloro-2-hydroxy-5-trimethylsilyl-4-pentyne 
• 148516-14-7 (S)-2-(3-trimethylsilyl-2-propynyl)oxirane 
• 143724-92-9 (S)-1-Phenyl-1-phenylsulfanyl-hex-5-yn-3-ol 
• 143724-91-8 (S)-1-Phenyl-1-phenylsulfanyl-6-trimethylsilanyl-hex-5-yn-3-ol 
• 143724-94-1 (Z)-(S)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-enoic acid methyl ester 
• 143724-93-0 (S)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-ynoic acid methyl ester 
• 143724-95-2 (R)-6-(2-Phenyl-2-phenylsulfanyl-ethyl)-5,6-dihydro-pyran-2-one 
• 143724-90-7 (2R)-1-chloro-5-(trimethylsilyl)pent-4-yn-2-ol 
• 143724-89-4 Trimethyl-((R)-3-oxiranyl-prop-1-ynyl)-silane 
• 143724-92-9 (R)-1-Phenyl-1-phenylsulfanyl-hex-5-yn-3-ol 
• 143724-91-8 (R)-1-Phenyl-1-phenylsulfanyl-6-trimethylsilanyl-hex-5-yn-3-ol 
• 143724-94-1 (Z)-(R)-5-Hydroxy-7-phenyl-7-phenylsulfanyl-hept-2-enoic acid methyl ester 

Downstream Products

• 122046-62-2 (S)-goniothalamin 
• 143724-97-4 (1R,4S,6R)-4-((E)-Styryl)-3,7-dioxa-bicyclo[4.1.0]heptan-2-one 
• 22639-28-7 (R)-goniothalamin 

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.