60603-14-7

Basic information

• Product Name: Cyclobutanone, 2-(phenylthio)-
• CAS NO: 60603-14-7
• Molecular Formula: C10H10OS
• Molecular Weight: 178.255
• Mol File: 60603-14-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclobutanone, 2-(phenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclobutanone, 2-(phenylthio)-(60603-14-7)
• EPA Substance Registry System: Cyclobutanone, 2-(phenylthio)-(60603-14-7)

Safety Data

• Hazardous Substances Data: 60603-14-7(Hazardous Substances Data)

Upstream product

• 84525-30-4 trans-2-phenylthiocyclobutanol 
• 1192-01-4 2-bromocyclobutanone 
• 930-69-8 sodium thiophenolate 
• 70871-28-2 1,2-bis(phenylthio)-1-cyclobutene 
• 108-98-5 thiophenol 
• 1191-95-3 cyclobutanone 
• 882-33-7 diphenyldisulfane 
• 84525-10-0 Benzoic acid (1S,2S)-2-phenylsulfanyl-cyclobutyl ester 
• 53480-95-8 1,1,4,4-tetrakis(phenylthio)butane 
• 84525-09-7 trans-2-phenylthiocyclobutyl acetate 

Downstream Products

• 80404-79-1 1-Furan-2-yl-4-phenylsulfanyl-butan-1-one 
• 98678-19-4 4-(phenylthio)-4-allyl-trans-decahydro-1-naphthalenone 
• 98678-12-7 4-(phenylthio)-4-allyl-trans-decahydro-1-naphthalenone 
• 98678-17-2 cis-4-(phenylthio)-trans-decahydro-1-naphthalenone 
• 98678-09-2 trans-4-(phenylthio)-trans-decahydro-1-naphthalenone 
• 98678-18-3 4-(phenylthio)-cis-decahydro-1-naphthalenone 
• 98678-11-6 2-allyl-2-(phenylthio)-1-(1-cyclohexenyl)cyclobutanol 
• 98678-24-1 3-(phenylthio)-2,2-(dimethyl)cyclopentanone 
• 98678-25-2 2-benzyl-2-(phenylthio)cyclobutanone 
• 98678-20-7 2-allyl-2-(phenylthio)cyclobutanone 
• 80404-71-3 2-Methyl-2-phenylsulfanyl-cyclobutanone 
• 80404-77-9 1-Cyclohexyl-2-phenylsulfanyl-cyclobutanol 
• 60603-15-8 1-methoxy-2-phenylthiocyclobutene 
• 98678-05-8 (E)-2-(phenylthio)-1-vinylcyclobutanol 

Relevant articles and documents

Enantioselective Construction of Sulfur-Containing Tetrasubstituted Stereocenters via Asymmetric Functionalizations of α-Sulfanyl Cyclic Ketones

Asymmetric functionalizations of α-sulfanyl cyclic ketones were realized via chiral phosphoric acid catalyzed enantioselective addition reactions with aldimines, azodicarboxylates and allenamides. A series of chiral organosulfur compounds possessing sulfur-containing tetrasubstituted stereocenters were accessed via these methods, with excellent regioselectivities and high stereoselectivities. (Figure presented.).

Phasentransfer-Katalyse zur Herstellung von α-Alkyl(Aryl)mercapto-Carbonylverbindungen

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An economical and convenient preparation of 2-(phenylthio)cyclobutanone, a synthetic equivalent of cyclobutanone

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