CAS 137-07-5

2-Aminothiophenol

Description:

2-Aminothiophenol, also known as 2-mercaptoaniline, is an organic compound characterized by the presence of both an amino group (-NH2) and a thiol group (-SH) attached to a thiophene ring. Its molecular structure consists of a six-membered aromatic ring containing sulfur, which contributes to its unique chemical properties. This compound is typically a solid at room temperature and is known for its potential applications in various fields, including pharmaceuticals, dyes, and as a precursor in organic synthesis. 2-Aminothiophenol exhibits moderate solubility in polar solvents due to the presence of the amino group, while its thiol functionality allows for the formation of disulfide bonds and other thiol-related reactions. It is important to handle this compound with care, as it may pose health risks, including skin and respiratory irritation. Additionally, it can undergo oxidation, leading to the formation of disulfides or other derivatives, making it a versatile reagent in chemical reactions.

Formula: C₆H₇NS

InChI: InChI=1S/C6H7NS/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2

InChI key: InChIKey=VRVRGVPWCUEOGV-UHFFFAOYSA-N

SMILES: NC1=C(S)C=CC=C1

Synonyms:

• 1-Amino-2-mercaptobenzene
• 2-Amino Thiophenol
• 2-Amino-1-mercaptobenzene
• 2-Aminobencenotiol
• 2-Aminobenzenethiol
• 2-Aminobenzenethiol Hydrochloride (1:1)
• 2-Aminobenzenethiolate
• 2-Aminobenzolthiol
• 2-Aminophenyl mercaptan
• 2-Mercaptoaniline
• 2-Thioaniline
• Benzenethiol, 2-amino-
• Benzenethiol, o-amino-
• Nsc 106635
• O-Aminothiophenol
• o-Aminobenzenethiol
• o-Aminophenyl mercaptan
• o-Mercaptoaniline

2-Aminobenzenethiol

CAS: 137-07-5

Formula: C₆H₇NS

Purity: >97.0%(T)

Color and Shape: Light yellow to Yellow to Orange clear liquid

Molecular weight: 125.19

Ref: 3B-A0267

2-Aminothiophenol, 98%

CAS: 137-07-5

2-Aminothiophenol was used in the synthesis of 1,5-benzothiazepines derivatives by reacting with 1,3-diphenylpropenone derivatives and using aluminosilicate solid catalysts. It was also used in the synthesis of benzothiazole2 and 3-(benzothiazol-2-yl)coumarin derivatives. The ternary complexes of co

Formula: C₆H₇NS

Purity: 98%

Color and Shape: Crystals or powder or crystalline powder or fused solid or clear liquid as melt, Yellow to brown

Molecular weight: 125.19

Ref: 02-A18952

2-Aminothiophenol

CAS: 137-07-5

Formula: C₆H₇NS

Color and Shape: Light yellow to yellow or orange liquid

Molecular weight: 125.19

Ref: 7W-GK7188

2-Aminothiophenol

CAS: 137-07-5

Formula: C₆H₇NS

Purity: 98.0%

Color and Shape: Low Melting Solid

Molecular weight: 125.19

Ref: 10-F002470

Dotinurad Impurity 13

CAS: 137-07-5

Formula: C₆H₇NS

Molecular weight: 125.19

Ref: 4Z-D-273015

2-Aminothiophenol

CAS: 137-07-5

2-Aminothiophenol

Formula: C₆H₇NS

Purity: 98%

Color and Shape: clear. yellow liquid

Molecular weight: 125.19g/mol

Ref: 54-OR1999

2-Aminothiophenol 90%

Controlled Product

CAS: 137-07-5

Stability Air Sensitive
Applications A multifunctional compound which shows antioxidant activity in a skin cell model of UVA-induced stress.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Sies, H., et al.: Eur. J. Biochem., 215, 213 (1993), Meotti, F., et al.: Environ. Res., 94, 276 (2004),

Formula: C₆H₇NS

Purity: 90%

Color and Shape: Neat

Molecular weight: 125.19

Ref: TR-A630425

2-Aminothiophenol

CAS: 137-07-5

2-Aminothiophenol is a chemical compound that belongs to the class of thiophenols and can be prepared by reacting sodium carbonate with hydrochloric acid. It has been shown to be an effective inhibitor of human immunoglobulin production in colorectal adenocarcinoma cells. 2-Aminothiophenol also inhibits the growth of bacteria, fungi, and some viruses. This compound binds to proteins by nucleophilic displacement of sulfur groups from cysteine residues on protein molecules, forming covalent bonds between amino groups and sulfur atoms. 2-Aminothiophenol has been used as a fluorescent derivative for the detection of disulfide bonds in proteins. The reaction mechanism is the same as that for other thiols: formation of a sulfenic acid intermediate followed by reduction to form disulfides. Analysis can be done using electrochemical impedance spectroscopy (EIS) or adsorption methods such as gas

Formula: C₆H₇NS

Purity: Min. 95%

Molecular weight: 125.18 g/mol

Ref: 3D-FA07685