CAS 367-34-0
:2,4,5-Trifluoroaniline
Description:
2,4,5-Trifluoroaniline is an aromatic amine characterized by the presence of three fluorine atoms attached to the benzene ring at the 2, 4, and 5 positions, along with an amino group (-NH2). This compound is typically a colorless to pale yellow solid at room temperature and is known for its moderate solubility in water, as well as higher solubility in organic solvents. The presence of fluorine atoms significantly influences its chemical properties, including increased electronegativity and altered reactivity compared to non-fluorinated anilines. 2,4,5-Trifluoroaniline is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and dyes. It is important to handle this compound with care, as it may pose health risks, including potential toxicity and environmental hazards. Proper safety measures should be taken when working with this substance, including the use of personal protective equipment and adherence to relevant regulations regarding chemical handling and disposal.
Formula:C6H4F3N
InChI:InChI=1S/C6H4F3N/c7-3-1-5(9)6(10)2-4(3)8/h1-2H,10H2
InChI key:InChIKey=QMYVWJVVVMIBMM-UHFFFAOYSA-N
SMILES:FC1=C(F)C=C(N)C(F)=C1
Synonyms:- 2,4,5-Trifluorobenzenamine
- 2,4,5-Trifluorophenylamine
- Ai3-52252
- Aniline, 2,4,5-trifluoro-
- Benzenamine, 2,4,5-trifluoro-
- NSC 10289
- 2,4,5-Trifluoroaniline
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Found 6 products.
2,4,5-Trifluoroaniline
CAS:Formula:C6H4F3NPurity:>98.0%(GC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:147.102,4,5-Trifluoroaniline
CAS:<p>2,4,5-Trifluoroaniline</p>Formula:C6H4F3NPurity:98%Color and Shape:Off-White SolidMolecular weight:147.10g/mol2,4,5-Trifluoroaniline
CAS:<p>2,4,5-Trifluoroaniline (TFAA) is a synthetic chemical that belongs to the class of electrophiles. It is a hydrogenation reduction product of 2,4,5-trichloroaniline and is used as an antibacterial agent. TFAA inhibits bacterial growth by reacting with thiols in proteins and nucleic acids. This compound has shown efficiencies on the order of 99% against gram positive bacteria and 95% against gram negative bacteria. TFAA also has been shown to inhibit the production of hydrogen sulfide in Escherichia coli and Pseudomonas aeruginosa. The biological properties of TFAA are due to its ability to bind to copper ions and undergo reductive elimination or substitution reactions. The crystal structure of TFAA has been determined using x-ray diffraction techniques. In this work, it was found that TFAA adopts a planar geometry with D2d symmetry at room temperature and melts</p>Formula:C6H4F3NPurity:Min. 95%Color and Shape:PowderMolecular weight:147.10 g/mol





