66660-08-0

Basic information

• Product Name: Benzene, [(3-iodopropyl)thio]-
• CAS NO: 66660-08-0
• Molecular Formula: C9H11IS
• Molecular Weight: 278.157
• Mol File: 66660-08-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, [(3-iodopropyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(3-iodopropyl)thio]-(66660-08-0)
• EPA Substance Registry System: Benzene, [(3-iodopropyl)thio]-(66660-08-0)

Safety Data

• Hazardous Substances Data: 66660-08-0(Hazardous Substances Data)

Upstream product

• 4911-65-3 3-chloropropyl phenyl sulfide 
• 930-69-8 sodium thiophenolate 
• 627-30-5 1-chloro-3-hydroxypropane 
• 627-31-6 1,3-Diiodopropane 
• 108-98-5 thiophenol 

Downstream Products

• 133188-98-4 3-(3-Phenylthiopropyl)-2-cyclohexen-1-one 
• 874-79-3 phenyl(propyl)sulfide 
• 29193-72-4 ethyl 4-(phenylthio)butanoate 
• 55129-89-0 1,4-bis(phenylthio)hexane 
• 110361-59-6 2-Oxo-5-phenylsulfanylmethyl-cyclopentanecarboxylic acid ethyl ester 
• 110361-58-5 3-Oxo-1-phenyl-4,5,6,7-tetrahydro-3H-1λ⁴-thiepine-2-carboxylic acid ethyl ester 
• 110361-66-5 (E)-3-Hydroxy-2-phenylsulfanyl-hepta-2,6-dienoic acid ethyl ester 
• 141649-93-6 5-Carboethoxy-5-hexenyl phenyl sulfoxide 
• 64740-40-5 phenyl (4-phenylbutyl) sulfide 
• 13910-16-2 n-octylsulfanylbenzene 
• 99965-76-1 6-(phenylthio)hexanenitrile 
• 141649-89-0 (E)-Ethyl 6-Phenylthio-2-hexenoate 
• 141649-90-3 (Z)-Ethyl 3-carboethoxy-6-phenylthio-2-hexenoate 
• 141649-92-5 4-Phenyl-7-phenylthio-2-heptanone 

Relevant articles and documents

Functionalized organolithium compounds: Generation via reductive lithiation and nucleophilic addition to N-phenethylimides. Access to functionalized dihydropyrrolo[2,1-a]isoquinolinones

A procedure for producing 1,4-dianion equivalents consists of reductive lithiation, induced by 4,4-di-tert-butylbiphenylide, of functionalized phenyl sulfides. Nucleophilic addition of 4-lithio-2-(trimelhylsilylmethyl)but-1- ene 1 and 2-(3-lithiopropyl)-2

Preparation and reactivity of polyfunctional zinc and copper organometallics bearing sulfur functionalities

Iodomethylthiobenzoate 5 and α-chloroalkyl phenyl sulfides 6 were found to insert zinc dust in THF under very mild conditions (10-25°C, 0.5-2 h) leading to zinc α-thioorganometallics. After a transmetallation with CuCN·2 LiCl, the corresponding copper rea