82420-76-6

Basic information

• Product Name: 2-[(naphthalen-2-yl)sulfanyl]-1-phenylethanone
• Synonyms: 2-[(naphthalen-2-yl)sulfanyl]-1-phenylethanone
• CAS NO: 82420-76-6
• Molecular Weight: 278.375
• Mol File: 82420-76-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-[(naphthalen-2-yl)sulfanyl]-1-phenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(naphthalen-2-yl)sulfanyl]-1-phenylethanone(82420-76-6)
• EPA Substance Registry System: 2-[(naphthalen-2-yl)sulfanyl]-1-phenylethanone(82420-76-6)

Safety Data

• Hazardous Substances Data: 82420-76-6(Hazardous Substances Data)

Upstream product

• 1021-45-0 phosphoric acid diethyl ester-(1-phenyl-vinyl ester) 
• 91-60-1 2-Naphthalenethiol 
• 98-88-4 benzoyl chloride 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 
• 36452-23-0 N-(phenylthio)-ε-caprolactam 
• 93-08-3 methyl 2-naphthyl ketone 
• 70-11-1 α-bromoacetophenone 
• 532-27-4 1-chloroacetophenone 
• 39689-37-7 sodium salt of β-mercaptonaphthalene 

Downstream Products

• 1046758-78-4 2,2-difluoro-2-(naphthalen-2-ylsulfonyl)-1-phenylethan-1-one 
• 158752-55-7 2-(naphthalen-2-ylsulfonyl)-1-phenylethan-1-one 
• 7381-78-4 1-phenyl-1-(α-naphthyl)ethane 
• 36707-32-1 1-(1-naphthyl)-2-phenylethane 
• 1248588-16-0 3-ethoxy-2-[(naphthalen-2-yl)sulfanyl]-1-phenylprop-2-en-1-one 
• 38226-58-3 2-(naphthalen-2-ylsulfinyl)-1-phenylethan-1-one 
• 882430-07-1 (R)-2-naphthyl phenacyl sulfoxide 
• 101722-95-6 2-(phenyl)-β-hydroxyethyl 2-napthyl sulfide 
• 16587-59-0 3-phenylnaphtho[2,1-b]thiophene 
• 16587-38-5 2-phenylnaphtho<2,1-b>thiophene 

Relevant articles and documents

Catalyst-Free Difunctionalization of Activated Alkenes in Water: Efficient Synthesis of β-Keto Sulfides and Sulfones

Difunctionalization of activated alkenes, a powerful strategy in chemical synthesis, has been accomplished for direct synthesis of a series of β-keto sulfides and β-keto sulfones. The transformation, mediated by O2, proceeds smoothly in water and without any catalyst. Prominent advantages of this method include mild reaction conditions, purification simplicity, and gram-scale synthesis, underlining the practical utility of this methodology.

Regioselective synthesis of 5-(arylsulfanyl)- and 5-(benzylsulfanyl)-6- phenylsalicylates by one-pot cyclizations of 1,3-bis(silyloxy)buta-1,3-dienes with 2-(arylsulfanyl)- and 5-(benzylsulfanyl)-3-ethoxy-1-phenylprop-2-en-1-ones

5-(Arylsulfanyl)-6-phenylsalicylates were prepared by one-pot cyclizations of 1,3-bis(trimethylsilyloxy) buta-1,3-dienes with 2-(arylsulfanyl)-3-ethoxy-1- phenylprop-2-en-1-ones.

α-Fluorination of β-ketosulfones by Selectfluor F-TEDA-BF4

Attempted fluorination of β-ketosulfides using Selectfluor resulted only in the isolation of the corresponding diaryl disulfides, presumed to arise by decomposition of an unstable fluorinated intermediate. However, fluorination of β-ketosulfones using Selectfluor under anhydrous conditions does allow the isolation of both mono-and difluorinated products in moderate to good yields.