81471-22-9

Basic information

• Product Name: 2-((1H-indol-3-yl)thio)benzoic acid
• Synonyms: 2-((1H-indol-3-yl)thio)benzoic acid
• CAS NO: 81471-22-9
• Molecular Weight: 269.324
• Mol File: 81471-22-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-((1H-indol-3-yl)thio)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((1H-indol-3-yl)thio)benzoic acid(81471-22-9)
• EPA Substance Registry System: 2-((1H-indol-3-yl)thio)benzoic acid(81471-22-9)

Safety Data

• Hazardous Substances Data: 81471-22-9(Hazardous Substances Data)

Upstream product

• 1484-27-1 3-bromoindole 
• 134-23-6 sodium thiosalicylate 
• 116757-21-2 methyl 2-((1H-indol-3-yl)thio)benzoate 
• 5459-63-2 bis[2-(methoxycarbonyl)phenyl]disulfide 
• 120-72-9 indole 
• 119-80-2 2,2'-dithiobenzoic acid 

Relevant articles and documents

Catalyst-free system for sulfenylation of free (N-H) indoles with 2,2′-dithiosalicylic acid under alkaline conditions

A catalyst-free system for the sulfenylation of free (N-H) indoles using 2,2′-dithiosalicylic acid under alkaline conditions was developed in this study. This system provides a green, convenient and efficient method for sulfenylindole synthesis, with good yields and high selectivity. This simple synthesis was performed in a green solvent (isopropanol/H2O) under atmospheric and catalyst-free conditions. The procedure was suitable for use with N-unprotected indoles. An electrophilic coupling mechanism was proposed.

Metal free sulfenylation and bis-sulfenylation of indoles: Persulfate mediated synthesis

A method which avoids metal and halogen for the synthesis of 3-arylthioindoles from indoles and diaryl disulfides using ammonium persulfate in methanol has been presented. Moreover, double C-H sulfenylation of indoles at 2 and 3-positions has also been ac

[1]Benzothieno[3,2-b]thiochromones and thiochromono[3,2-b]indoles

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