64001-48-5

Basic information

• Product Name: Benzoyl chloride, 2-(sulfinylamino)-
• Synonyms: N-sulfinyl-anthraniloyl chloride;2-Thionylamino-benzoylchlorid;N-Sulfinyl-anthraniloylchlorid
• CAS NO: 64001-48-5
• Molecular Formula: C7H4ClNO2S
• Molecular Weight: 201.633
• Mol File: 64001-48-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 2-(sulfinylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2-(sulfinylamino)-(64001-48-5)
• EPA Substance Registry System: Benzoyl chloride, 2-(sulfinylamino)-(64001-48-5)

Safety Data

• Hazardous Substances Data: 64001-48-5(Hazardous Substances Data)

Upstream product

• 7719-09-7 thionyl chloride 
• 118-92-3 anthranilic acid 

Downstream Products

• 123767-94-2 anthraniloyl chloride ; hydrochloride 
• 340291-84-1 2-(2-amino-benzoylamino)-5-benzyloxybenzoic acid methyl ester 
• 49854-16-2 methyl 2-(2-aminobenzoylamino)benzoate 
• 134-20-3 2-carbomethoxyaniline 
• 331758-78-2 3-(4-methylphenyl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one 
• 15351-42-5 dianthranilide 
• 1009318-28-8 3-(2-methoxyphenyl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one 
• 18189-02-1 propan-2-yl 2-aminobenzoate 
• 21132-01-4 2,3-diphenyl-2,3-dihydro-1H-quinazolin-4-one 
• 63384-39-4 3-(4-chlorophenyl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one 
• 7756-96-9 n-butyl anthranilate 
• 61554-52-7 2-(2-bromomethyl-4-oxo-4H-quinazolin-3-yl)-benzoic acid methyl ester 
• 2006-80-6 2-(2-methyl-4-oxo-4H-quinazoline-3-yl)benzoic acid methyl ester 
• 340291-81-8 2-[2-(N-benzyloxycarbonyl-L-alanyl)benzoylamino]benzoic acid methyl ester 

Relevant articles and documents

On the reaction of anthranilic acid with thionyl chloride: The actual structure of 'Kametani's sulfinamide anhydride'

Despite previous reports, no sulfinamide anhydride is formed from the reaction of anthranilic acid with thionyl chloride, the actual product being 2-sulfinylaminobenzoyl chloride. This excludes iminoketene formation in the reactions of this activated form

Efficient syntheses of 2,3-disubstituted natural quinazolinones via iridium catalysis

Natural products sclerotigenin, pegamine, deoxyvasicinone, mackinazolinone, and rutaecarpine were synthesized. Core quinazolinone structures were constructed via Ir catalysis. The Royal Society of Chemistry 2012.

On the reaction of anthranilic acid with thionyl chloride: Iminoketene intermediate formation

2-(Sulfinylamino) benzoyl chloride is formed on treating anthranilic acid with thionyl chloride. The formation of iminoketene intermediate from 2-(sulfinylamino) benzoyl chloride is established and the reactions carried out using the intermediate are described.