81358-55-6

Basic information

• Product Name: 2-Pentanone, 5-(phenylthio)-
• CAS NO: 81358-55-6
• Molecular Formula: C11H14OS
• Molecular Weight: 194.298
• Mol File: 81358-55-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-Pentanone, 5-(phenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pentanone, 5-(phenylthio)-(81358-55-6)
• EPA Substance Registry System: 2-Pentanone, 5-(phenylthio)-(81358-55-6)

Safety Data

• Hazardous Substances Data: 81358-55-6(Hazardous Substances Data)

Upstream product

• 97600-68-5 5-phenylthiopentan-2-one ethylene acetal 
• 882-33-7 diphenyldisulfane 
• 66080-23-7 4,4,5,5-tetramethyl-2-((phenylsulfanyl)methyl)-1,3,2-dioxaborolane 
• 78-94-4 methyl vinyl ketone 
• 100-68-5 methyl-phenyl-thioether 
• 765-43-5 Cyclopropyl methyl ketone 
• 108-98-5 thiophenol 
• 3884-71-7 bromo-5-pentanone-2 
• 1192-40-1 copper(I) thiophenolate 
• 5891-21-4 5-chloro-2-pentanone 
• 930-69-8 sodium thiophenolate 
• 3128-06-1 5-ketohexanoic acid 
• 5978-08-5 1-chloro-4-(1,3-dioxolane)-n-pentane 

Downstream Products

• 97600-70-9 3-methyl-3-(3-phenylthiopropyl)oxepin-2(3H)-one 
• 477482-18-1 3-methyl-6-(phenylthio)hex-1-en-3-ol 
• 223266-05-5 1,5-bis(phenylthio)2-methylpent-1-ene 
• 162661-38-3 (S)-5-Phenylsulfanyl-pentan-2-ol 
• 87143-63-3 5-Phenylsulfanyl-oct-7-en-2-one 
• 97600-69-6 6-methyl-6-(3-phenylthiopropyl)fulvene 
• 77970-55-9 5-(phenylsulfonyl)pentan-2-one 

Relevant articles and documents

Ring-Opening Reactions of Electrophilic Cyclopropanes

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Process for alkylation of group VI compound

The invention provides a process for alkylation of a group VI compound. Under an illumination condition, an active ester with a general formula of Ra-COONPhth and a main group VI compound with a general formula of Rb-A-Rc undergo the following reaction un

Organic photocatalysis for the radical couplings of boronic acid derivatives in batch and flow

We report an acridium-based organic photocatalyst as an efficient replacement for iridium-based photocatalysts to oxidise boronic acid derivatives by a single electron process. Furthermore, we applied the developed catalytic system to the synthesis of four active pharmaceutical ingredients (APIs). A straightforward scale up approach using continuous flow photoreactors is also reported affording gram an hour throughput.