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[ CAS No. 1196-57-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1196-57-2
Chemical Structure| 1196-57-2
Structure of 1196-57-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1196-57-2 ]

CAS No. :1196-57-2 MDL No. :MFCD00006722
Formula : C8H6N2O Boiling Point : -
Linear Structure Formula :C6H4N2C2H(OH) InChI Key :FFRYUAVNPBUEIC-UHFFFAOYSA-N
M.W : 146.15 Pubchem ID :14526
Synonyms :
Chemical Name :2-Quinoxalinol

Calculated chemistry of [ 1196-57-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 41.56
TPSA : 46.01 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.3 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.52
Log Po/w (XLOGP3) : 1.25
Log Po/w (WLOGP) : 1.34
Log Po/w (MLOGP) : 0.66
Log Po/w (SILICOS-IT) : 1.5
Consensus Log Po/w : 1.25

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.21
Solubility : 0.909 mg/ml ; 0.00622 mol/l
Class : Soluble
Log S (Ali) : -1.81
Solubility : 2.24 mg/ml ; 0.0153 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.73
Solubility : 0.272 mg/ml ; 0.00186 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.77

Safety of [ 1196-57-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1196-57-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 1196-57-2 ]
  • Downstream synthetic route of [ 1196-57-2 ]

[ 1196-57-2 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 34836-97-0 ]
  • [ 1196-57-2 ]
  • [ 2427-71-6 ]
Reference: [1] Heterocycles, 1985, vol. 23, # 1, p. 143 - 151
  • 2
  • [ 1196-57-2 ]
  • [ 2427-71-6 ]
Reference: [1] Chemistry Letters, 1984, p. 323 - 326
  • 3
  • [ 34836-97-0 ]
  • [ 1196-57-2 ]
  • [ 2427-71-6 ]
  • [ 89938-22-7 ]
  • [ 6639-79-8 ]
Reference: [1] Heterocycles, 1985, vol. 23, # 1, p. 143 - 151
  • 4
  • [ 1196-57-2 ]
  • [ 25652-34-0 ]
  • [ 6272-25-9 ]
Reference: [1] Patent: US5153196, 1992, A,
  • 5
  • [ 1196-57-2 ]
  • [ 6272-25-9 ]
Reference: [1] Journal of Medicinal Chemistry, 1992, vol. 35, # 18, p. 3319 - 3324
[2] Bioorganic Chemistry, 2014, vol. 56, p. 16 - 26
  • 6
  • [ 1196-57-2 ]
  • [ 6272-25-9 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 5, p. 1403 - 1407
[2] Journal of Medicinal Chemistry, 2011, vol. 54, # 13, p. 4508 - 4522
  • 7
  • [ 1196-57-2 ]
  • [ 89898-96-4 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 2007, vol. 55, # 2, p. 255 - 267
[2] Yakugaku Zasshi, 1959, vol. 79, p. 658[3] Chem.Abstr., 1959, p. 21979
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