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2-Ethoxybenzamide

Synopsis, Chemistry

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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

2-Ethoxybenzamide

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 Formula	C₉H₁₁NO₂
Molecular Weight	165.19 g/mol
XLogP3	1.2
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	3
Exact Mass	165.078978594 g/mol
Monoisotopic Mass	165.078978594 g/mol
Topological Polar Surface Area	52.3 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	159
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

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