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1 References  














Butyrophenone






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From Wikipedia, the free encyclopedia
 


Butyrophenone
Names
Preferred IUPAC name

1-Phenylbutan-1-one

Identifiers

CAS Number

3D model (JSmol)

  • Interactive image
  • ChEMBL
    ChemSpider
    ECHA InfoCard 100.007.091 Edit this at Wikidata

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C10H12O/c1-2-6-10(11)9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3 checkY

      Key: FFSAXUULYPJSKH-UHFFFAOYSA-N checkY

    • InChI=1/C10H12O/c1-2-6-10(11)9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3

      Key: FFSAXUULYPJSKH-UHFFFAOYAC

    • O=C(c1ccccc1)CCC

    • CCCC(=O)c1ccccc1

    Properties

    Chemical formula

    C10H12O
    Molar mass 148.20 g/mol
    Appearance clear liquid
    Melting point 12 °C (54 °F; 285 K)
    Boiling point 229 °C (444 °F; 502 K)

    Solubility in water

    poor
    log P 2.77

    Refractive index (nD)

    1.520
    Hazards
    NFPA 704 (fire diamond)
    NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
    1
    1
    1
    Flash point 99 °C (210 °F; 372 K)

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    checkY verify (what is checkY☒N ?)

    Infobox references

    Butyrophenone is an organic compound with the formula C6H5C(O)C3H7. It is a colorless liquid.

    The butyrophenone structure—a ketone flanked by a phenyl ring and a butyl chain—forms the basis for many other chemicals containing various substituents. Some of these butyrophenones are used to treat various psychiatric disorders such as schizophrenia, as well as acting as antiemetics.[1]

    Examples of butyrophenone-derived pharmaceuticals include:

    References[edit]

    1. ^ a b c Keith Parker; Laurence Brunton Goodman; Louis Sanford; Lazo, John S.; Gilman, Alfred (2006). Goodman & Gilman's The Pharmacological Basis of Therapeutics (11th ed.). New York: McGraw-Hill. ISBN 0071422803.
  • ^ Grogan, Charles H.; Rice, Leonard M. (1967). "Ω-Azabicyclic Butyrophenones". Journal of Medicinal Chemistry. 10 (4): 621–623. doi:10.1021/jm00316a022. PMID 6037051.
  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Butyrophenone&oldid=1198097292"

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    Aromatic ketones
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