CAS 14371-82-5

2-Nitro-4-(trifluoromethyl)benzenethiol

Description:

2-Nitro-4-(trifluoromethyl)benzenethiol, with the CAS number 14371-82-5, is an organic compound characterized by the presence of a thiol (-SH) group attached to a benzene ring that also features a nitro group (-NO2) and a trifluoromethyl group (-CF3). This compound typically exhibits a yellow to brown color and is known for its strong odor. The presence of the trifluoromethyl group enhances its lipophilicity and can influence its reactivity and interaction with biological systems. The nitro group contributes to the compound's electron-withdrawing properties, which can affect its acidity and overall chemical behavior. As a thiol, it can participate in redox reactions and form disulfides, making it relevant in various chemical syntheses and applications. Additionally, the compound may exhibit antimicrobial or antifungal properties, making it of interest in pharmaceutical and agricultural research. Safety precautions should be taken when handling this substance, as it may pose health risks due to its reactive nature and potential toxicity.

Formula: C₇H₄F₃NO₂S

InChI: InChI=1S/C7H4F3NO2S/c8-7(9,10)4-1-2-6(14)5(3-4)11(12)13/h1-3,14H

InChI key: InChIKey=HUJMWBOFGAQSMR-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=CC(C(F)(F)F)=CC=C1S

Synonyms:

• 2-Nitro-4-(trifluoromethyl)benzene-1-thiol
• p-Toluenethiol, α,α,α-trifluoro-2-nitro-
• Benzenethiol, 2-nitro-4-(trifluoromethyl)-
• 2-Nitro-4-trifluoromethylthiophenol
• 2-Nitro-4-(trifluoromethyl)benzenethiol

2-nitro-4-(trifluoromethyl)benzenethiol

CAS: 14371-82-5

Formula: C₇H₄F₃NO₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 223.1724

Ref: IN-DA001I8U

2-Nitro-4-(trifluoromethyl)thiophenol

CAS: 14371-82-5

2-Nitro-4-(trifluoromethyl)thiophenol

Purity: ≥95%

Color and Shape: Solid

Molecular weight: 223.17g/mol

Ref: 54-PC1551

2-Nitro-4-(trifluoromethyl)benzenethiol

CAS: 14371-82-5

2-Nitro-4-(trifluoromethyl)benzenethiol is an organic compound that contains a sulfur atom in its molecular structure. It is used as an antiparasitic agent and has been shown to have potentiating effects on platelet aggregation. This molecule can be synthesized by reacting thiosemicarbazide with a trifluoromethylsilane and a nitroalkane. The nucleophilic nature of the trifluoromethyl group enables this reaction, which produces 2-Nitro-4-(trifluoromethyl)benzenethiol and 2-aminothiophenol. 2-Nitro-4-(trifluoromethyl)benzenethiol has also been shown to have etiological properties, which may be due to the nitro group.

Formula: C₇H₄F₃NO₂S

Purity: 95%Min

Molecular weight: 223.17 g/mol

Ref: 3D-FN84821