13165-80-5

Basic information

• Product Name: 2-sulfinobenzoic acid
• CAS NO: 13165-80-5
• Molecular Formula: C₇H₆O₄S
• Molecular Weight: 186.1851
• Mol File: 13165-80-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 488.6°C at 760 mmHg
• Flash Point: 249.3°C
• Density: 1.7g/cm³
• Vapor Pressure: 2.33E-10mmHg at 25°C
• Refractive Index: 1.728
• CAS DataBase Reference: 2-sulfinobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-sulfinobenzoic acid(13165-80-5)
• EPA Substance Registry System: 2-sulfinobenzoic acid(13165-80-5)

Safety Data

• Hazardous Substances Data: 13165-80-5(Hazardous Substances Data)

Upstream product

• 66650-27-9 1,1-dichloro-1λ⁴-benz[c][1,2]oxathiol-3-one 
• 124-38-9 carbon dioxide 
• 94600-72-3 N-(phenylsulfinyl)-N-(tert-butyl)amine 
• 147-93-3 Thiosalicylic acid 
• 91837-36-4 3H-2,1-benzoxathiolan-3-one 1-oxide 
• 118-92-3 anthranilic acid 
• 40625-64-7 2-chlorosulfinylbenzoyl chloride 
• 101349-96-6 2-chloromethanesulfonyl-benzoic acid 

Downstream Products

• 412300-93-7 2-(2-oxo-2-phenyl-ethanesulfonyl)-benzoic acid phenacyl ester 
• 861080-05-9 2-(3,4-dioxo-3,4-dihydro-naphthalene-1-sulfinyl)-benzoic acid 
• 861080-02-6 2-(2,5-dihydroxy-benzenesulfonyl)-benzoic acid 
• 492-22-8 thio-xanthene-9-one 
• 4892-02-8 Methyl thiosalicylate 
• 5459-63-2 bis[2-(methoxycarbonyl)phenyl]disulfide 
• 63114-30-7 (3-hydroxy-1,1-dioxo-1λ⁶-benzo[b]thiophen-2-yl)-phenyl ketone 
• 412300-96-0 2-[(4-nitro-phenyl)-methanesulfonyl]-benzoic acid-(4-nitro-benzyl ester) 
• 131223-31-9 2-(4'-nitrobenzylsulfonyl)benzoic acid 
• 25700-42-9 2-(Pentafluorbenzylsulfonyl)-benzoesaeure 
• 147-93-3 Thiosalicylic acid 
• 1906-41-8 2-<<(2-carboxyphenyl)sulfonyl>thio>benzoic acid 
• 119-80-2 2,2'-dithiobenzoic acid 
• 632-25-7 2-sulfobenzoic acid 

Relevant articles and documents

Directed ortho lithiation of N-tert-butylbenzenesulfinamide

Introducing the sulfinamide group as a new useful ortho-directing group, we are presenting the synthesis of a series of ortho-substituted N-tert-butylbenzenesulfinamides via directed lithiation of the title compound and subsequent quenching of the dilithiated intermediates with various electrophiles.

SULFUR HETEROCYCLES. 12. REACTIONS OF CYCLIC ANHYDRIDES OF β-SULFINOCARBOXYLIC ACIDS WITH NUCLEOPHILES

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