57774-95-5

Basic information

• Product Name: 5-(phenylsulfanyl)pentan-1-ol
• CAS NO: 57774-95-5
• Molecular Formula: C₁₁H₁₆OS
• Molecular Weight: 196.3091
• Mol File: 57774-95-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 316.3°C at 760 mmHg
• Flash Point: 154°C
• Density: 1.06g/cm³
• Vapor Pressure: 0.000175mmHg at 25°C
• Refractive Index: 1.559
• CAS DataBase Reference: 5-(phenylsulfanyl)pentan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(phenylsulfanyl)pentan-1-ol(57774-95-5)
• EPA Substance Registry System: 5-(phenylsulfanyl)pentan-1-ol(57774-95-5)

Safety Data

• Hazardous Substances Data: 57774-95-5(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 2100-17-6 4-pentenal 
• 74203-20-6 5-benzoyloxy-1-iodopentane 
• 55162-82-8 1-benzoyloxypentan-5-ol 
• 111-29-5 1 ,5-pentanediol 
• 923571-44-2 benzoic acid 5-methanesulfonyloxy-pentyl ester 
• 923571-34-0 benzoic acid 5-phenylsulfanyl-pentyl ester 
• 4285-51-2 pent-4-en-1-yl phenyl sulfide 
• 102438-33-5 5-(phenylthio)pentanal 
• 20965-36-0 2-(phenylthio)tetrahydro-2H-pyran 
• 5259-98-3 5-chloropentan-1-ol 

Downstream Products

• 923571-35-1 1-Methoxy-4-(5-phenylsulfanyl-pentyloxymethyl)-benzene 
• 49638-99-5 5-Benzenesulfinyl-5-chloro-pentan-1-ol 
• 57774-96-6 7-Methyl-1-phenyl-7-aza-1-thiooctan 
• 99965-78-3 6,6-bis(phenylthio)hexanenitrile 
• 99965-77-2 6-chloro-6-(phenylthio)hexanenitrile 
• 99965-76-1 6-(phenylthio)hexanenitrile 
• 37053-16-0 cyclopent-1-en-1-yl (phenyl) sulfide 
• 121942-47-0 11-Benzenesulfonyl-15-(tert-butyl-dimethyl-silanyloxy)-10-methanesulfonyloxy-pentadecanoic acid methyl ester 
• 121942-46-9 11-Benzenesulfonyl-15-(tert-butyl-dimethyl-silanyloxy)-10-hydroxy-pentadecanoic acid methyl ester 
• 121942-43-6 11-Benzenesulfonyl-15-(tert-butyl-dimethyl-silanyloxy)-pentadecanoic acid methyl ester 
• 121942-42-5 (5-Benzenesulfonyl-pentyloxy)-tert-butyl-dimethyl-silane 
• 106-02-5 pentadecanolide 
• 180259-48-7 1-methoxy-4-((pent-4-en-1-yloxy)methyl)benzene 
• 132047-92-8 tert-butyl(pent-4-en-1-yloxy)diphenylsilane 

Relevant articles and documents

Mild preparation of alkenes from phenyl sulfides: One-pot elimination of phenylthio group via sulfilimine at ambient temperature

(Chemical Equation Presented) Various alkenes were prepared from phenyl sulfides in a one-pot manner at room temperature by converting them to the corresponding S-aminosulfonium salts with O-mesitylenesulfonylhydroxylamine, followed by treatment with pota

Synthese de lactones a cycle moyen: Application a la synthese du pentadecanolide-15 et du phoracantholide I

Medium ring size lactones can be prepared from bifunctional commercial starting compounds in high yields, using a few step sequence.Lactonisation is obtained by cyclization of the free ω-hydroxyacids or by the cyclization of ω-hydroxyacids having the hydroxy and carboxy group protected.

Epoxyannulation. 4. Reactions of 1,5-, 1,6-, and 1,7-Oxosulfonium Salts

Treatment of six 1,5- and 1,6-oxosulfonium salts with potassium tert-butoxide affords an oxabicyclohexane, an oxabicycloheptane, hydrindan oxides, or a decalin oxide in 55-95percent yield.The stereoselectivity of this reaction ranges from 75percent for the formation of (1α,3α,7α)-2-oxatricyclo1,3>decane (21) to greater 99percent for (1α,2α,7α)-2-oxatricyclo1,3>decane (14) and for (1α,2α,8β)-2-oxatricyclo1,3>undecane (25).Five 1,7-oxosulfonium salts, one 1,8-salt, and one 1,11-salt and base give only elimination products.The sulfonium salt from 2-cyclopentanone (29) provides 3-methylspirodec-2-en-6-one (30) in 40percent yield.The salt from 2-cyclohexanone (32) yields 38percent of 4-methylbicycloundeca-1(7),3,5-triene (33).