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CAS 5761-97-7

:

Methylphenylphosphinic chloride

Description:
Methylphenylphosphinic chloride, with the CAS number 5761-97-7, is an organophosphorus compound characterized by the presence of a methyl group and a phenyl group attached to a phosphinic acid moiety. This compound typically appears as a colorless to pale yellow liquid and is known for its reactivity due to the presence of the chloride functional group, which can participate in nucleophilic substitution reactions. Methylphenylphosphinic chloride is soluble in organic solvents, making it useful in various chemical syntheses and applications, particularly in the production of phosphinic acid derivatives. It is important to handle this compound with care, as it may pose health hazards, including irritation to the skin, eyes, and respiratory system. Additionally, it can be toxic if ingested or inhaled, necessitating appropriate safety measures during handling and storage. Overall, methylphenylphosphinic chloride serves as a valuable intermediate in organic synthesis and materials science, contributing to the development of various chemical products.
Formula:C7H8ClOP
InChI:InChI=1/C7H8ClOP/c1-10(8,9)7-5-3-2-4-6-7/h2-6H,1H3
SMILES:CP(=O)(c1ccccc1)Cl
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Found 2 products.
  • Methylphenylphosphinic Chloride
    Indagoo
    + Info

    Methylphenylphosphinic Chloride

    CAS:
    Formula:C7H8ClOP
    Color and Shape:Liquid
    Molecular weight:174.5646

    Ref: IN-DA003S48

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  • Methyl(phenyl)phosphinoyl chloride
    Biosynth
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    Methyl(phenyl)phosphinoyl chloride

    CAS:

    Methyl(phenyl)phosphinoyl chloride is a phosphorus-containing compound that is an intermediate in the synthesis of the drug phosphinothioyl chloride. Methyl(phenyl)phosphinoyl chloride is used in the treatment of hepatitis, but it also has antiviral properties. The enantiomers of methyl(phenyl)phosphinoyl chloride have different effects on viruses. The left-handed enantiomer inhibits RNA polymerase and other enzymes involved in virus replication, while the right-handed enantiomer blocks virus assembly. Magnetic resonance spectroscopy (MRS) analysis has shown that the left-handed enantiomer binds to the receptor for growth factor, which may account for its antiviral activity.

    Formula:C7H8ClOP
    Purity:Min. 95%
    Molecular weight:174.56 g/mol

    Ref: 3D-FAA76197

    10g
    489.00€