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Overview of CAS 501-94-0

Client Email Product
4CN-0970
PharmaCompass
4CN-0970
Also known as: 2-(4-hydroxyphenyl)ethanol, 501-94-0, 4-hydroxyphenethyl alcohol, 4-(2-hydroxyethyl)phenol, 4-hydroxyphenylethanol, 4-hydroxybenzeneethanol
Molecular Formula
C8H10O2
Molecular Weight
138.166  g/mol
InChI Key
YCCILVSKPBXVIP-UHFFFAOYSA-N
FDA UNII
1AK4MU3SNX

1 2D Structure

4CN-0970

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
4-(2-hydroxyethyl)phenol
2.1.2 InChI
InChI=1S/C8H10O2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10H,5-6H2
2.1.3 InChI Key
YCCILVSKPBXVIP-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1=CC(=CC=C1CCO)O
2.2 Other Identifiers
2.2.1 UNII
1AK4MU3SNX
2.3 Synonyms
2.3.1 Depositor-Supplied Synonyms

1. 2-(4-hydroxyphenyl)ethanol

2. 501-94-0

3. 4-hydroxyphenethyl Alcohol

4. 4-(2-hydroxyethyl)phenol

5. 4-hydroxyphenylethanol

6. 4-hydroxybenzeneethanol

7. P-hydroxyphenethyl Alcohol

8. Benzeneethanol, 4-hydroxy-

9. P-tyrosol

10. P-hydroxyphenylethanol

11. 4-hydroxyphenylethyl Alcohol

12. 2-(4-hydroxyphenyl)ethyl Alcohol

13. P-thyrosol

14. Nsc 59876

15. P-hpea

16. 2-(p-hydroxyphenyl)ethanol

17. 4-hydroxyphenethylalcohol

18. Einecs 207-930-8

19. P-hydroxyphenylethyl Alcohol

20. 4-(2-hydroxy-ethyl)-phenol

21. Chembl53566

22. Chebi:1879

23. 2-(4-hydroxyphenyl)ethan-1-ol

24. Yccilvskpbxvip-uhfffaoysa-n

25. Mfcd00002902

26. 2-(4-hydroxyphenyl)ethanol (tyrosol)

27. St51045473

28. Smr000857159

29. Unii-1ak4mu3snx

30. Beta-(4-hydroxyphenyl)ethanol

31. 4-tyrosol

32. Phep

33. 4-hydroxybenzenethanol

34. Pubchem9418

35. 4-(hydroxyethyl)phenol

36. P-hydroxy-benzeneethanol

37. 4-hydroxy-benzeneethanol

38. Ac1q7cjn

39. 1ak4mu3snx

40. Acmc-1awq1

41. B-(p-hydroxyphenyl)ethanol

42. Bmse000173

43. Ac1l1v3q

44. B-(4-hydroxyphenyl)ethanol

45. 4-hydroxyphenylmethylcarbinol

46. 2-(p-hydroxyphenyl) Ethanol

47. Schembl43838

48. (4-hydroxyphenethyl) Alcohol

49. 2-(4-hydroxyphenyl) Ethanol

50. 2-(4-hydroxyphenyl)-ethanol

51. Beta-(p-hydroxyphenyl)ethanol

52. Ksc270m5j

53. Mls001332423

54. Mls001332424

55. Phenethyl Alcohol, P-hydroxy-

56. Ac1q7a89

57. Ethanol, 2-(4-hydroxyphenyl)

58. Dtxsid8060111

59. Schembl10620528

60. .beta.-(p-hydroxyphenyl)ethanol

61. 2-(4-hydroxyphenyl)-1-ethanol

62. Ctk1h0654

63. Ethanol, 2-(4-hydroxyphenyl)-

64. .beta.-(4-hydroxyphenyl)ethanol

65. Molport-000-139-897

66. Otava-bb 1204410

67. Akos 91052

68. Hms2230e12

69. Zinc164581

70. 2-(4-hydroxyphenyl)ethanol, 98%

71. 4-hydroxyphenethyl Alcohol; Tyrosol

72. Nsc59876

73. Str02735

74. Anw-30928

75. Bdbm50339585

76. Nsc-59876

77. Sbb086008

78. Akos000280287

79. Ac-2493

80. As00553

81. Cm10966

82. Cs-w019782

83. Ebd1837856

84. Ks-5274

85. Mcule-9268661621

86. Rp20448

87. Ks-0000019m

88. Tra-0177328

89. Ncgc00246994-01

90. 4cn-0970

91. Aj-16220

92. Ak-35340

93. An-13934

94. Bc676907

95. Br-35340

96. Bt000148

97. Cj-02176

98. Kb-71460

99. Or012492

100. Or190128

101. Or190129

102. Or274369

103. Sc-15906

104. Sy001653

105. Zb008209

106. Ab1004194

107. Db-019455

108. Db-050520

109. Kb-192756

110. Kb-222884

111. Ls-167639

112. St2416119

113. Tl8003328

114. Tx-018167

115. Am20060146

116. Ft-0082985

117. Ft-0608647

118. N1496

119. C06044

120. M-6239

121. 2-(4-hydroxyphenyl)ethanol, Analytical Standard

122. I01-1942

123. F0001-1309

124. 947d0361-23c6-4863-8346-22ab05108ac5

125. 4-hydroxy-benzeneethanol;4-hydroxyphenylethanol;beta-(4-hydroxyphenyl)ethanol

126. Inchi=1/c8h10o2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10h,5-6h

127. Yrl

2.4 Create Date
2005-03-26
3 Chemical and Physical Properties
Molecular Weight 138.166 g/mol
Molecular Formula C8H10O2
XLogP30.4
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass138.068 g/mol
Monoisotopic Mass138.068 g/mol
Topological Polar Surface Area40.5 A^2
Heavy Atom Count10
Formal Charge0
Complexity85.3
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

Antioxidants

Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues.


Anti-Arrhythmia Agents

Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade.


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