70042-49-8

Basic information

• Product Name: α-<1-(phenylthio)cyclopropyl>benzyl alcohol
• Synonyms: α-<1-(phenylthio)cyclopropyl>benzyl alcohol
• CAS NO: 70042-49-8
• Molecular Weight: 256.368
• Mol File: 70042-49-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: α-<1-(phenylthio)cyclopropyl>benzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: α-<1-(phenylthio)cyclopropyl>benzyl alcohol(70042-49-8)
• EPA Substance Registry System: α-<1-(phenylthio)cyclopropyl>benzyl alcohol(70042-49-8)

Safety Data

• Hazardous Substances Data: 70042-49-8(Hazardous Substances Data)

Upstream product

• 124479-81-8 α-(1-(phenylsulfinyl)cyclopropyl)benzyl alcohol 
• 100-52-7 benzaldehyde 
• 50337-59-2 cyclopropyl phenyl sulfoxide 
• 28118-53-8 1,3-bis(phenylthio)propane 
• 14633-54-6 cyclopropylphenylsulfide 

Downstream Products

• 144453-25-8 2-phenyl-1-(phenylthio)cyclobutene 
• 144453-32-7 3-phenyl-2-(phenylthio)-1,3-butadiene 
• 42436-86-2 2-phenylcyclobutanone 
• 122732-92-7 1,1-di(phenylthio)-2-phenylcyclobutane 
• 127560-54-7 C₂₂H₂₀S₂ 

Relevant articles and documents

A Novel Route to Geminal Dibromocyclobutanes: Syntheses of 2-Substituted Cyclobutanone Acetals and Their Reaction with Boron Tribromide

Nine 2-substituted cyclobutanone acetals, in addition to the parent cyclobutanone acetal, were synthesized from their corresponding cyclobutanones and subsequently treated with boron tribromide. The substituents were either alkyl chains or a phenyl and a

FLUORIDE-CATALYZED CONDENSATION OF 1-PHENYLSULFINYL-1-(TRIMETHYLSILYL)CYCLOPROPANE WITH CARBONYL COMPOUNDS

1-Phenylsulfinyl-1-(trimethylsilyl)cyclopropane reacts with aldehydes in the presence of Bu4NF to give 1-phenylsulfinyl-1-(α-hydroxyalkyl)cyclopropanes.

A New and Convenient Synthetic Method for Cyclopropyl Phenyl Sulfides

The reactions of a variety of 1,3-bis(phenylthio)propanes with butyllithium have been shown to produce cyclopropyl phenyl sulfides in good to high yields.A new and convenient in situ preparation of 1-lithiocyclopropyl phenyl sulfide can be readily carried out by treating 1,3-bis(phenylthio)propane with 2 equiv. of butyllithium at 0 degC in THF.The reaction with electrophiles proceeds in good yield.O-Aryl and O-alkyl S-cyclopropyl dithiocarbonates also can be prepared in good yields. 1,2-Bis(phenylthio)ethane was converted to phenyl vinyl sulfide on treatment with butyllithium, while 1,4-bis(phenylthio)butane was recovered unchanged by a similar treatment.