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    2-Ethoxybenzamide

    ACTIVE PHARMA INGREDIENTS

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

    ANALYTICAL

    PharmaCompass
    $ API Ref.Price (USD/KG) : 112Xls

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    2D Structure
    Also known as: 2-ethoxybenzamide, 938-73-8, O-ethoxybenzamide, Benzamide, 2-ethoxy-, Etenzamide, Ethbenzamide
    Molecular Formula
    C9H11NO2
    Molecular Weight
    165.19  g/mol
    InChI Key
    SBNKFTQSBPKMBZ-UHFFFAOYSA-N
    FDA UNII
    L929ZCK4BF
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    2-ethoxybenzamide
    2.1.2 InChI
    InChI=1S/C9H11NO2/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6H,2H2,1H3,(H2,10,11)
    2.1.3 InChI Key
    SBNKFTQSBPKMBZ-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CCOC1=CC=CC=C1C(=O)N
    2.2 Other Identifiers
    2.2.1 UNII
    L929ZCK4BF
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 2-ethoxy-benzamide

    2. 2-ethoxybenzamide

    3. O-ethoxybenzamide

    2.3.2 Depositor-Supplied Synonyms

    1. 2-ethoxybenzamide

    2. 938-73-8

    3. O-ethoxybenzamide

    4. Benzamide, 2-ethoxy-

    5. Etenzamide

    6. Ethbenzamide

    7. Ethenzamid

    8. Etamide

    9. Anovigam

    10. Ethosalicyl

    11. Lucamide

    12. Pirosolvina

    13. Etosalicil

    14. Etosalicyl

    15. Katagrippe

    16. Protopyrin

    17. Trancalgyl

    18. Etocil

    19. Eusal

    20. Benzamide, O-ethoxy-

    21. Nsc 28787

    22. H.p. 209

    23. Nsc-28787

    24. L929zck4bf

    25. J3.352i

    26. Ncgc00091616-01

    27. Ethenzamide 100 Microg/ml In Acetonitrile

    28. Dsstox_cid_581

    29. Dsstox_rid_75671

    30. Dsstox_gsid_20581

    31. Etenzamide [dcit]

    32. Etenzamida

    33. Ethenzamidum

    34. Etenzamida [inn-spanish]

    35. Ethenzamidum [inn-latin]

    36. 2-eethoxybenzamide

    37. Cas-938-73-8

    38. Ccris 9124

    39. Einecs 213-346-4

    40. Unii-l929zck4bf

    41. Brn 2208582

    42. Ethanzamide

    43. Ethenzamide [inn:ban:jan]

    44. Orthoethoxybenzamide

    45. Ethenzamide (tn)

    46. 2-ethoxybenzoylamide

    47. Mfcd00007977

    48. Ethenzamide [mi]

    49. Ethenzamide [inn]

    50. Ethenzamide [jan]

    51. 2-ethoxybenzamide, 97%

    52. Wln: Zvr Bo2

    53. Ethenzamide (jp17/inn)

    54. Ethenzamide [mart.]

    55. Schembl25624

    56. Ethenzamide [who-dd]

    57. 4-10-00-00175 (beilstein Handbook Reference)

    58. Mls002302987

    59. Zinc1384

    60. Chembl1483877

    61. Dtxsid4020581

    62. Chebi:31564

    63. Hms3039j16

    64. Ethenzamide 1.0 Mg/ml In Methanol

    65. Hy-b1428

    66. Nsc28787

    67. Tox21_111156

    68. Tox21_200025

    69. S4524

    70. Stk105005

    71. Akos003280312

    72. Tox21_111156_1

    73. Ccg-213844

    74. Cs-4916

    75. Db13544

    76. Ks-5320

    77. Ncgc00091616-02

    78. Ncgc00091616-03

    79. Ncgc00257579-01

    80. Ac-11991

    81. Smr001307304

    82. Db-057442

    83. E0222

    84. Ft-0612206

    85. D01466

    86. D70657

    87. Ab01010349_03

    88. A844727

    89. Q553324

    90. Sr-01000877236

    91. Q-201075

    92. Sr-01000877236-2

    93. Z54953371

    2.4 Create Date
    2005-03-25
    3 Chemical and Physical Properties
    Molecular Weight 165.19 g/mol
    Molecular Formula C9H11NO2
    XLogP31.2
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count3
    Exact Mass165.078978594 g/mol
    Monoisotopic Mass165.078978594 g/mol
    Topological Polar Surface Area52.3 Ų
    Heavy Atom Count12
    Formal Charge0
    Complexity159
    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

    Anti-Inflammatory Agents, Non-Steroidal

    Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)

    4.2 ATC Code

    N - Nervous system

    N02 - Analgesics

    N02B - Other analgesics and antipyretics

    N02BA - Salicylic acid and derivatives

    N02BA07 - Ethenzamide