7686-29-5

Basic information

• Product Name: 2-amino-4-nitrobenzenethiol
• Synonyms: 2-amino-4-nitrobenzenethiol
• CAS NO: 7686-29-5
• Molecular Formula: C₆H₆N₂O₂S
• Molecular Weight: 170.18904
• Mol File: 7686-29-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 108 °C
• Boiling Point: 366.3±27.0 °C(Predicted)
• Appearance: /
• Density: 1.465±0.06 g/cm3(Predicted)
• PKA: 6.19±0.10(Predicted)
• CAS DataBase Reference: 2-amino-4-nitrobenzenethiol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4-nitrobenzenethiol(7686-29-5)
• EPA Substance Registry System: 2-amino-4-nitrobenzenethiol(7686-29-5)

Safety Data

• Hazardous Substances Data: 7686-29-5(Hazardous Substances Data)

Usage

Appearance

Yellow solid

Solubility

Insoluble in water

Common use

Organic synthesis

Composition

Thiol derivative of nitroaniline

Functional groups

Nitro group and amino group attached to a benzene ring

Application

Building block in the synthesis of pharmaceuticals, dyes, and other organic compounds

Biological activity

Some biological activity and potential medical applications.

Upstream product

• 2218-96-4 2,4-dinitrothiophenol 
• 15620-71-0 N_.N-Dimethylthiocarbamidsaeure-S-(2.4-dinitrophenylester) 
• 51-28-5 2,4-Dinitrophenol 
• 369-36-8 6-fluoro-3-nitroaniline 
• 10403-47-1 2-bromo 5-nitroaniline 
• 6283-25-6 H₂NC₆H₃(Cl)NO₂ 

Downstream Products

• 13599-78-5 5-Nitro-1,2,3-benzothiadiazol 
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• 845658-37-9 2-benzyl-5-nitro-1,3-benzothiazole 
• 21762-74-3 6-nitro-3,4-dihydro-3-oxo-2H(1,4)benzothiazine 
• 945533-85-7 N-(2-(4-chlorophenyl)benzo[d]thiazol-5-yl)isobutyramide 
• 43087-94-1 2-(4-chlorophenyl)benzo[d]thiazol-5-amine 
• 1215113-39-5 2-(4-chlorophenyl)-5-nitrobenzo[d]thiazole 
• 136775-81-0 5-nitro-2-(4-methylphenyl)-benzothiazole 
• 873984-37-3 bis-(2-benzoylamino-4-nitro-phenyl)-disulfide 
• 64448-50-6 5-nitro-2-phenyl-benzothiazole 

Relevant articles and documents

Selective reduction of nitroaromatic compounds on silver nanoparticles by visible light

For the first time, we report experimentally and theoretically that nitroaromatic compounds, 2,4-dinitrobenzenethiol and 4-chloro-2- nitrobenzenethiol, on silver sols can be selectively reduced to 2-amino-4-nitrobenzenethiol and 2-amino-4-chlorobenzenethiol simply by irradiating with a visible light in ambient conditions, and the selective photoreduction is a very facile process. The results of quantum chemical calculations are in good agreement with our experimental data. Copyright

Alpha2C adrenoreceptor agonists

In its many embodiments, the present invention relates to a novel class of phenylmorpholine and phenylthiomorpholine compounds useful as α2C adrenergic receptor agonists, pharmaceutical compositions containing the compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the α2C adrenergic receptor agonists using such compounds or pharmaceutical compositions.

Side chain polymers exhibiting nonlinear optical response

This invention provides novel side chain polymers which exhibit nonlinear optical response, and which have utility as a transparent optical component in all-optical and electrooptical light switch and light modulator devices. An invention side chain polymer is illustrated by the following structure: STR1