Cas no 69403-12-9 (2-Fluoro-4-(trifluoromethyl)aniline)

2-Fluoro-4-(trifluoromethyl)aniline is a fluorinated aromatic amine with the molecular formula C7H5F4N. This compound features both a fluorine substituent and a trifluoromethyl group on the aniline ring, enhancing its electron-withdrawing properties and making it a valuable intermediate in organic synthesis. Its structural features contribute to high reactivity in cross-coupling reactions, electrophilic substitutions, and as a building block for pharmaceuticals, agrochemicals, and advanced materials. The presence of fluorine atoms improves metabolic stability and lipophilicity in derived compounds. This product is typically supplied as a high-purity liquid or solid, ensuring consistent performance in research and industrial applications. Proper handling is required due to its potential toxicity and sensitivity to air and moisture.
2-Fluoro-4-(trifluoromethyl)aniline structure
69403-12-9 structure
Product Name:2-Fluoro-4-(trifluoromethyl)aniline
CAS No:69403-12-9
MF:C7H5F4N
MW:179.11491560936
CID:973662
Update Time:2025-05-26

2-Fluoro-4-(trifluoromethyl)aniline Chemical and Physical Properties

Names and Identifiers

    • l-phenylalanine dehydrogenase
    • L-Phenylalanine Dehydrogenase from Rhodococcus spec. M4
    • L-PHENYLALANINE DEHYDROGENASE FROM SPOROSARCINA SP LARGER THAN 6 U MG
    • Phenylalanine dehydrogenase
    • 2-fluoro-4-(trifluoromethyl)aniline
    • 4-Amino-3-fluorobenzotrifluoride
    • 3-FLUORO-4-AMINOBENZOTRIFLUORIDE
    • 2-fluoro-4-trifluoromethylaniline
    • Benzenamine, 2-fluoro-4-(trifluoromethyl)-
    • 2-FLUORO-4-(TRIFLUOROMETHYL)BENZENAMINE
    • 2-fluoro-4-(trifluoromethyl)phenylamine
    • 2-FLUORO-4-(TRIFLUORMETHYL)ANILINE
    • 4-Amino-3-fluorobenzotri-fluoride
    • PubChem2813
    • 2-(Benzoyloxymethyl)benzoicacid
    • a,a,a,2-Tetrafluoro-p-toluidine
    • Fluoro-4-(trifluoromethyl)aniline
    • WT395
    • 2-f
    • 2-Fluoro-4-(trifluoromethyl)aniline
    • Inchi: 1S/C7H5F4N/c8-5-3-4(7(9,10)11)1-2-6(5)12/h1-3H,12H2
    • InChI Key: ARHDUOQIXLGANT-UHFFFAOYSA-N
    • SMILES: FC1=C(C=CC(C(F)(F)F)=C1)N

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 156
  • XLogP3: 2.2
  • Topological Polar Surface Area: 26

2-Fluoro-4-(trifluoromethyl)aniline Security Information

  • WGK Germany:3

2-Fluoro-4-(trifluoromethyl)aniline Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd.
L920305-50U
L-PHENYLALANINE DEHYDROGENASE
69403-12-9
50U
¥5,737.50 2022-01-10

2-Fluoro-4-(trifluoromethyl)aniline Suppliers

Suzhou Senfeida Chemical Co., Ltd
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(CAS:69403-12-9)L-PHENYLALANINE DEHYDROGENASE
Order Number:sfd21838
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:39
Price ($):discuss personally

Additional information on 2-Fluoro-4-(trifluoromethyl)aniline

Introduction to 2-Fluoro-4-(trifluoromethyl)aniline (CAS No. 69403-12-9)

2-Fluoro-4-(trifluoromethyl)aniline (CAS No. 69403-12-9) is a versatile organic compound that has garnered significant attention in the fields of pharmaceuticals, agrochemicals, and materials science. This compound is characterized by its unique combination of a fluorine atom and a trifluoromethyl group attached to an aniline backbone, which imparts it with distinct chemical and physical properties. These properties make it an essential building block in the synthesis of various advanced materials and pharmaceutical intermediates.

The molecular structure of 2-Fluoro-4-(trifluoromethyl)aniline consists of a benzene ring with a fluorine atom at the 2-position and a trifluoromethyl group at the 4-position, along with an amino group (-NH2) attached to the benzene ring. The presence of these functional groups significantly influences the compound's reactivity and stability, making it highly suitable for a wide range of synthetic transformations.

In the pharmaceutical industry, 2-Fluoro-4-(trifluoromethyl)aniline is often used as an intermediate in the synthesis of drugs with potent biological activities. For instance, it has been utilized in the development of selective serotonin reuptake inhibitors (SSRIs), which are widely prescribed for treating depression and anxiety disorders. Recent studies have also explored its potential in the synthesis of novel antiviral agents, particularly those targeting viral proteases involved in the replication of RNA viruses such as influenza and SARS-CoV-2.

The unique electronic properties of 2-Fluoro-4-(trifluoromethyl)aniline make it an attractive candidate for use in materials science applications. Its ability to form stable complexes with various metal ions has led to its use in the development of luminescent materials and sensors. For example, researchers have synthesized coordination polymers using this compound as a ligand, which exhibit enhanced photoluminescence properties and can be used for detecting specific analytes in environmental monitoring.

In the agrochemical sector, 2-Fluoro-4-(trifluoromethyl)aniline has found applications in the synthesis of herbicides and fungicides. The introduction of fluorine atoms into these compounds can improve their selectivity and efficacy, reducing the environmental impact while maintaining high agricultural productivity. Recent advancements in green chemistry have also focused on developing more sustainable methods for synthesizing this compound, aiming to minimize waste and energy consumption during production processes.

The synthesis of 2-Fluoro-4-(trifluoromethyl)aniline typically involves multi-step reactions starting from readily available starting materials. One common approach is to use 4-trifluoromethylaniline as a starting point, followed by selective fluorination at the 2-position. Advances in catalytic methods have significantly improved the yield and purity of this compound, making it more accessible for industrial applications.

Safety considerations are paramount when handling 2-Fluoro-4-(trifluoromethyl)aniline. While it is not classified as a hazardous material under current regulations, proper safety protocols should be followed to ensure safe handling and storage. This includes using appropriate personal protective equipment (PPE) such as gloves and goggles, working in well-ventilated areas, and storing the compound away from incompatible substances.

In conclusion, 2-Fluoro-4-(trifluoromethyl)aniline (CAS No. 69403-12-9) is a valuable compound with diverse applications across multiple industries. Its unique chemical structure and properties make it an essential component in the development of advanced materials, pharmaceuticals, and agrochemicals. Ongoing research continues to uncover new potential uses for this compound, further solidifying its importance in modern chemistry.

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Suzhou Senfeida Chemical Co., Ltd
(CAS:69403-12-9)L-PHENYLALANINE DEHYDROGENASE
sfd21838
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
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