Cas no 77992-51-9 (Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]-)

Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- is a specialized hydrazine derivative featuring a bromo- and trifluoromethyl-substituted phenyl group. This compound is primarily utilized as a versatile intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. The presence of both bromo and trifluoromethyl functional groups enhances its reactivity, enabling selective transformations such as nucleophilic substitutions and cross-coupling reactions. Its structural features make it valuable for constructing complex molecules with tailored electronic and steric properties. The compound is typically handled under controlled conditions due to the reactivity of the hydrazine moiety. Suitable for research and industrial applications requiring precise functionalization.
Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- structure
77992-51-9 structure
Product Name:Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]-
CAS No:77992-51-9
MF:C7H6BrF3N2
MW:255.035151004791
CID:551300
PubChem ID:53426482
Update Time:2025-11-02

Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- Chemical and Physical Properties

Names and Identifiers

    • Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]-
    • [4-Bromo-3-(trifluoromethyl)phenyl]hydrazine
    • 4-Bromo-3-trifluoromethyl-phenyl-hydrazine
    • 3-(trifluoromethyl)-4-bromophenylhydrazine
    • 4-bromo-3-trifluoromethylphenyl-hydrazine
    • AG-H-12834
    • CTK5E5273
    • KB-240736
    • SureCN1593091
    • AKOS014182580
    • 77992-51-9
    • SCHEMBL1593091
    • YKXJXHVLEAPHFR-UHFFFAOYSA-N
    • 4-Isoxazolecarboxylic acid, 3-(4-fluorophenyl)-5-methyl-, ethyl ester
    • DTXSID50699241
    • (4-Bromo-3-(trifluoromethyl)phenyl)hydrazine
    • MDL： MFCD02663115
    • Inchi： 1S/C7H6BrF3N2/c8-6-2-1-4(13-12)3-5(6)7(9,10)11/h1-3,13H,12H2
    • InChI Key： YKXJXHVLEAPHFR-UHFFFAOYSA-N
    • SMILES： BrC1=CC=C(C=C1C(F)(F)F)NN

Computed Properties

  • Exact Mass: 253.96668
  • Monoisotopic Mass: 253.96665g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 174
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.7
  • Topological Polar Surface Area: 38?2

Experimental Properties

  • PSA: 38.05

Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- Pricemore >>

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Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- Related Literature

Additional information on Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]-

Comprehensive Guide to Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- (CAS No. 77992-51-9): Properties, Applications, and Market Insights

Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- (CAS No. 77992-51-9) is a specialized organic compound that has garnered significant attention in the chemical and pharmaceutical industries. Known for its unique molecular structure featuring a 4-bromo-3-(trifluoromethyl)phenyl group, this compound is widely utilized in synthetic chemistry and advanced material research. Its hydrazine moiety makes it particularly valuable for constructing nitrogen-containing heterocycles, which are crucial in drug development and agrochemical formulations.

One of the most searched questions about Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- revolves around its synthesis and stability. Researchers often inquire about optimal reaction conditions for its preparation, as well as its compatibility with other reagents. The compound’s trifluoromethyl group enhances its lipophilicity, making it a preferred intermediate in the design of bioactive molecules. Recent trends in AI-driven drug discovery have further amplified interest in such compounds, as they are frequently used in high-throughput screening and virtual library design.

In the pharmaceutical sector, Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- is employed as a key building block for small-molecule inhibitors targeting enzymes and receptors. Its bromo-substituted aromatic ring allows for further functionalization via cross-coupling reactions, a topic frequently explored in academic and industrial research. Given the rising demand for precision medicine and targeted therapies, this compound’s role in developing novel therapeutics cannot be overstated.

From an industrial perspective, Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- is also valued for its applications in material science. Its incorporation into polymers and coatings can impart unique properties such as enhanced thermal stability and chemical resistance. With the growing emphasis on sustainable chemistry, researchers are investigating greener synthesis routes for this compound to minimize environmental impact.

The market for Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- is projected to expand, driven by its versatility and the increasing need for advanced chemical intermediates. Companies specializing in custom synthesis and contract research are actively stocking this compound to meet the demands of pharmaceutical and agrochemical clients. Additionally, its relevance in catalysis and ligand design continues to attract attention from academic and industrial chemists alike.

In summary, Hydrazine,[4-bromo-3-(trifluoromethyl)phenyl]- (CAS No. 77992-51-9) is a multifaceted compound with broad applications in drug discovery, material science, and industrial chemistry. Its unique structural features and reactivity profile make it indispensable for researchers working on cutting-edge scientific challenges. As the fields of medicinal chemistry and green synthesis evolve, this compound is poised to remain a critical tool in the chemist’s arsenal.

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