31183-81-0

Basic information

• Product Name: 2-aMino-4-Methylbenzenethiol
• Synonyms: 2-aMino-4-Methylbenzenethiol
• CAS NO: 31183-81-0
• Molecular Formula: C₇H₉NS
• Molecular Weight: 139.21806
• EINECS: -0
• Mol File: 31183-81-0.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 255.5±20.0 °C(Predicted)
• Appearance: /
• Density: 1.154±0.06 g/cm3(Predicted)
• PKA: 8.53±0.11(Predicted)
• CAS DataBase Reference: 2-aMino-4-Methylbenzenethiol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-aMino-4-Methylbenzenethiol(31183-81-0)
• EPA Substance Registry System: 2-aMino-4-Methylbenzenethiol(31183-81-0)

Safety Data

• Hazardous Substances Data: 31183-81-0(Hazardous Substances Data)

Usage

Functional Group

Thiol (sulfur group bonded to a hydrogen and a benzene ring)

Applications

Organic synthesis
Pharmaceutical research (building block for medications and dyes)
Materials science (polymer and adhesive development)

Chemical Properties

Thiol group (-SH) provides nucleophilic and reducing properties
Benzene ring contributes to aromaticity and stability

Reactivity

Participates in nucleophilic substitution reactions
Can undergo oxidation to form disulfides

Utility in Research

Valuable reagent in the study of sulfur-containing compounds
Important in organic chemistry for synthesis purposes

Upstream product

• 89-60-1 1-chloro-4-methyl-2-nitro-benzene 
• 106-43-4 para-chlorotoluene 
• 95-26-1 2,5-dimethylbenzothiazole 
• 14779-17-0 2-amino-5-methylbenzothiazole 
• 4274-36-6 bis-(4-Methyl-2-nitrophenyl)-trisulfide 
• 31183-82-1 Bis-<2-amino-4-methyl-phenyl>-trisulfid 

Downstream Products

• 139331-51-4 2-{3-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-propyl}-6-methyl-4H-benzo[1,4]thiazin-3-one; hydrochloride 
• 40925-61-9 6-Methylbenzothiazolon 

Relevant articles and documents

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Catalytic enantioselective one-pot approach to cis- and trans-2,3-diaryl substituted 1,5-benzothiazepines

The first enantioselective catalytic approach to cis- and trans-2,3-diaryl substituted 1,5-benzothiazepines has been conveniently developed in a one-pot fashion, starting from α,β-unsaturated acyl pyrazoles and 2-aminothiophenol. The organocatalytic two-s

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