61485-96-9

Basic information

• Product Name: Benzoyl chloride, 2-[(4-methylphenyl)thio]-
• CAS NO: 61485-96-9
• Molecular Formula: C14H11ClOS
• Molecular Weight: 262.76
• Mol File: 61485-96-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 2-[(4-methylphenyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2-[(4-methylphenyl)thio]-(61485-96-9)
• EPA Substance Registry System: Benzoyl chloride, 2-[(4-methylphenyl)thio]-(61485-96-9)

Safety Data

• Hazardous Substances Data: 61485-96-9(Hazardous Substances Data)

Upstream product

• 15774-73-9 2-(4'-methylphenylsulfanyl)benzoic acid 
• 106-45-6 para-thiocresol 
• 118-92-3 anthranilic acid 

Downstream Products

• 65935-79-7 2-p-Tolylsulfanyl-benzoic acid p-tolyl ester 
• 65935-90-2 2-(Toluene-4-sulfinyl)-benzoic acid p-tolyl ester 
• 15774-73-9 2-(4'-methylphenylsulfanyl)benzoic acid 
• 65936-09-6 (2-Hydroxy-5-methyl-phenyl)-(2-p-tolylsulfanyl-phenyl)-methanone 
• 15774-82-0 2-methyl-9H-thioxanthen-9-one 
• 176509-28-7 (2-p-Tolylsulfanyl-benzoyl)-phosphonic acid dimethyl ester 
• 104351-53-3 N-Methoxy-2-p-tolylsulfanyl-benzamide 

Relevant articles and documents

Reactions of carbene intermediates from the reaction of trialkyl phosphites with dialkyl benzoylphosphonates: Intramolecular cyclisations of 2-substituted dialkyl benzoylphosphonates

The reaction of dialkyl benzoylphosphonates 1 with trialkyl phosphites leads to the formation of carbene intermediates 3 via the anionic intermediates 2. The carbene intermediates 3 (R = 2-PhO, 2-PhOCH2, and 2-PhS) have been generated by heating the corresponding 2-substituted dialkyl benzoylphosphonates with trimethyl phosphite and their subsequent reactions investigated. Reactions proceed either by intermolecular trapping of the carbene intermediates by trimethyl phosphite to give novel ylidic phosphonates 4, or by intramolecular routes involving carbene insertion into the π-system of the phenyl ring in the substituent. Studies using methyl-substituted derivatives have shown that the formation of the thioxanthenylphosphonate 15 (X = S, R′ = R″ = Me) proceeds via a spiro diene intermediate 14 (X = S, R′ = R″ = Me).