CAS 361-39-7

6-Nitro-2,4,5-trifluoroaniline

Description:

6-Nitro-2,4,5-trifluoroaniline is an organic compound characterized by its aromatic structure, which includes a nitro group and trifluoro substituents on an aniline backbone. The presence of the nitro group (-NO2) introduces a strong electron-withdrawing effect, influencing the compound's reactivity and properties. The trifluoro groups (-CF3) enhance the compound's lipophilicity and stability, making it less prone to hydrolysis compared to non-fluorinated analogs. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical properties make it of interest in various applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, due to the presence of both nitro and trifluoro groups, it may exhibit unique electronic and steric properties, which can be exploited in material science and chemical research. Safety precautions should be taken when handling this compound, as it may pose health risks, including potential toxicity.

2-Nitro-3,4,6-trifluoroaniline

CAS: 361-39-7

Formula: C₆H₃F₃N₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 192.0954

Ref: IN-DA00CKUC

3,4,6-Trifluoro-2-nitroaniline

CAS: 361-39-7

3,4,6-Trifluoro-2-nitroaniline

Purity: 95%

Molecular weight: 192.10g/mol

Ref: 54-PC901854

3,4,6-Trifluoro-2-nitroaniline

CAS: 361-39-7

Formula: C₆H₃F₃N₂O₂

Purity: 98%

Molecular weight: 192.097

Ref: 10-F459056

3,4,6-trifluoro-2-nitroaniline

CAS: 361-39-7

3,4,6-Trifluoro-2-nitroaniline is a chemical compound with the formula C6H3FN3O2. It is an organic nitro compound that contains a nitro group, which is a functional group consisting of an oxygen atom double bonded to a nitrogen atom. Nitro groups are used in organic chemistry as a replacement for hydrogen atoms in order to produce compounds that have similar properties to those of their parent hydrocarbon. Nitro groups can be introduced into organic molecules by diazotization and coupling reactions. Nitration and chlorination of 3,4,6-trifluoro-2-nitroaniline give C6H3ClFNO2 and C6H3ClFNO respectively. 3,4,6-Trifluoro-2-nitroaniline has been shown to react with hypophosphorous acid to form hypophosphorous acid fluoride (C6H5P

Formula: C₆H₃F₃N₂O₂

Purity: Min. 95%

Molecular weight: 192.1 g/mol

Ref: 3D-AAA36139