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    Benzarone

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    REF. STANDARDS & IMPURITIES

    PharmaCompass
    $ API Ref.Price (USD/KG) : 153Xls

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    2D Structure
    Also known as: 1477-19-6, (2-ethylbenzofuran-3-yl)(4-hydroxyphenyl)methanone, Vasoc, Fragivix, Venagil, Benzarona
    Molecular Formula
    C17H14O3
    Molecular Weight
    266.29  g/mol
    InChI Key
    RFRXIWQYSOIBDI-UHFFFAOYSA-N
    FDA UNII
    23ZW4BG89C
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    (2-ethyl-1-benzofuran-3-yl)-(4-hydroxyphenyl)methanone
    2.1.2 InChI
    InChI=1S/C17H14O3/c1-2-14-16(13-5-3-4-6-15(13)20-14)17(19)11-7-9-12(18)10-8-11/h3-10,18H,2H2,1H3
    2.1.3 InChI Key
    RFRXIWQYSOIBDI-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CCC1=C(C2=CC=CC=C2O1)C(=O)C3=CC=C(C=C3)O
    2.2 Other Identifiers
    2.2.1 UNII
    23ZW4BG89C
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Benzaron

    2. Ehbb

    2.3.2 Depositor-Supplied Synonyms

    1. 1477-19-6

    2. (2-ethylbenzofuran-3-yl)(4-hydroxyphenyl)methanone

    3. Vasoc

    4. Fragivix

    5. Venagil

    6. Benzarona

    7. Benzaronum

    8. Fagivil

    9. 2-ethyl-3-benzofuranyl P-hydroxyphenyl Ketone

    10. 2-ethyl-3-(4-hydroxybenzoyl)benzofuran

    11. Methanone, (2-ethyl-3-benzofuranyl)(4-hydroxyphenyl)-

    12. L 2197

    13. Nsc 82134

    14. 2-ethyl-3-(p-hydroxybenzoyl)benzofuran

    15. 2-ethyl-4'-hydroxy-3-benzoylbenzofuran

    16. (2-ethyl-1-benzofuran-3-yl)-(4-hydroxyphenyl)methanone

    17. Nsc-82134

    18. Ketone, 2-ethyl-3-benzofuranyl P-hydroxyphenyl

    19. 23zw4bg89c

    20. Benzaron

    21. Chembl1474963

    22. Fragivil

    23. Chebi:34559

    24. Benzofuran, (2-ethyl-3-(4'-hydroxybenzoyl))

    25. Nsc82134

    26. (2-ethyl-1-benzofuran-3-yl)(4-hydroxyphenyl)methanone

    27. L-2197

    28. Benzarone [inn:dcf]

    29. (2-ethylbenzofuran-3-yl)(4-hydroxyphenyl)methanone (benzarone)

    30. Benzaronum [inn-latin]

    31. Benzarona [inn-spanish]

    32. L 2197-labaz

    33. Benzofuran, [2-ethyl-3-(4'-hydroxybenzoyl)]

    34. Einecs 216-026-2

    35. L 2179-labaz

    36. Brn 0222901

    37. Unii-23zw4bg89c

    38. 2-ethyl-3-(4'-hydroxybenzoyl)benzofuran

    39. Ethyl-2 (hydroxy-4 Benzoyl)-3 Benzofuranne [french]

    40. Benzarone [inn]

    41. Benzarone [mi]

    42. Ethyl-2 (hydroxy-4 Benzoyl)-3 Benzofuranne

    43. Benzarone [mart.]

    44. Zinc71

    45. Benzarone [who-dd]

    46. Nciopen2_004472

    47. 5-18-02-00334 (beilstein Handbook Reference)

    48. Mls006010019

    49. Schembl555497

    50. (2-ethylbenzofuran-3-yl)-(4-hydroxyphenyl)methanone

    51. Dtxsid2061721

    52. Ex-a1132

    53. Wln: T56 Boj C2 Dor Dq

    54. 2-ethyl-3-p-hydroxybenzoylbenzofuran

    55. Bdbm50342278

    56. Mfcd00867417

    57. Akos016010825

    58. Hy-w011711

    59. Ac-36827

    60. As-18081

    61. Smr001550644

    62. E1289

    63. Unm000003519301

    64. F17414

    65. 477b196

    66. Sr-01000945019

    67. (2-ethyl-3-benzofuranyl)(4-hydroxyphenyl)methanone

    68. [[4-(1-methyl-1-phenylethyl)phenoxy]methyl]-oxiran

    69. Sr-01000945019-1

    70. Q27116149

    71. (2-ethyl-benzofuran-3-yl)-(4-hydroxy-phenyl)-methanone

    72. (2-ethylbenzo[b]furan-3-yl)(4-hydroxyphenyl)methanone

    2.4 Create Date
    2005-03-26
    3 Chemical and Physical Properties
    Molecular Weight 266.29 g/mol
    Molecular Formula C17H14O3
    XLogP34.3
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count3
    Rotatable Bond Count3
    Exact Mass266.094294304 g/mol
    Monoisotopic Mass266.094294304 g/mol
    Topological Polar Surface Area50.4 Ų
    Heavy Atom Count20
    Formal Charge0
    Complexity346
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Fibrinolytic Agents

    Fibrinolysin or agents that convert plasminogen to FIBRINOLYSIN. (See all compounds classified as Fibrinolytic Agents.)