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5-Methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone

Compound 5-methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone, also known as fluvoxamineone, CAS number 61718-80-7, has the following uses:
Key intermediate in the synthesis of fluvoxamine: This compound is a key intermediate in the synthesis of fluvoxamine, a selective serotonin reuptake inhibitor (SSRI) that is widely used in the treatment of depression, obsessive-compulsive disorder and other mental disorders.

    Basic information

    Product Name: 5-Methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone
    Synonyms: 
    CAS: 61718-80-7
    MF: C13H15F3O2
    MW: 260.25

    Chemical Properties

    Boiling Point: 318.7±42.0 °C(Predicted)
    Density: 1.147±0.06 g/cm3(Predicted)
    storage temp: Sealed in dry,Room Temperature
    Solubility: Chloroform (Slightly), Methanol (Slightly)
    Form: NA
    Pka: NA
    Color: NA
    InChI: NA
    InChIKey: NA
    SMILES: NA

    product description

    Synthesis of antimicrobial drugs: As a prodrug of tedizolid, tedizolid phosphate can be rapidly converted into biologically active tedizolid by phosphatase in vivo for the treatment of acute bacterial skin tissue infection in adults caused by gram-positive bacteria.
    Scientific research reagents: widely used in molecular biology, pharmacology and other scientific research fields, is an indispensable reagent in scientific research, but it is strictly forbidden to use it in the human body.
    Pharmacokinetic studies: In clinical trials, the pharmacokinetic profile of tedizolid phosphate is studied to evaluate its efficacy and safety in treatment.
    Antimicrobial activity study: Tedizolid phosphate also has strong in vitro antibacterial activity against some vancomycin and linezolid-resistant strains, providing a new option against drug-resistant strains.
    Treatment of acute bacterial skin and skin soft tissue infections (ABSSSI): Tedizolid phosphate is indicated for the treatment of ABSSSI caused by susceptible strains, including infections caused by methicillin-resistant Staphylococcus aureus (MRSA).
    Drug Interaction Studies: Compared with linezolid, tedizolid phosphate does not exhibit similar drug-drug interactions, providing patients with a safer treatment option.
    Antimicrobial drug development: As a new oxazolidinone antibiotic, tedizolid phosphate has the advantages of strong antibacterial activity, high oral bioavailability and long half-life, and is an ideal antibacterial drug.

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