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[ CAS No. 23082-50-0 ] {[proInfo.proName]}

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Chemical Structure| 23082-50-0
Chemical Structure| 23082-50-0
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Product Details of [ 23082-50-0 ]

CAS No. :23082-50-0 MDL No. :MFCD00052836
Formula : C8H6ClNO3 Boiling Point : -
Linear Structure Formula :- InChI Key :PNXVQYABDFYOFY-UHFFFAOYSA-N
M.W : 199.59 Pubchem ID :89996
Synonyms :

Calculated chemistry of [ 23082-50-0 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 50.47
TPSA : 62.89 Ų

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) : -5.97 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.39
Log Po/w (XLOGP3) : 2.18
Log Po/w (WLOGP) : 2.45
Log Po/w (MLOGP) : 1.18
Log Po/w (SILICOS-IT) : 0.65
Consensus Log Po/w : 1.57

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.66
Solubility : 0.436 mg/ml ; 0.00219 mol/l
Class : Soluble
Log S (Ali) : -3.13
Solubility : 0.147 mg/ml ; 0.000734 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.73
Solubility : 0.367 mg/ml ; 0.00184 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.8

Safety of [ 23082-50-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 23082-50-0 ]

* 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 [ 23082-50-0 ]
  • Downstream synthetic route of [ 23082-50-0 ]

[ 23082-50-0 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 23082-50-0 ]
  • [ 90764-90-2 ]
Reference: [1] Journal of Medicinal Chemistry, 2003, vol. 46, # 26, p. 5663 - 5673
  • 2
  • [ 23082-50-0 ]
  • [ 40621-84-9 ]
Reference: [1] Journal of Medicinal Chemistry, 2003, vol. 46, # 26, p. 5663 - 5673
  • 3
  • [ 23082-50-0 ]
  • [ 5757-85-7 ]
Reference: [1] Patent: EP2773638, 2015, B1,
  • 4
  • [ 23082-50-0 ]
  • [ 35272-19-6 ]
Reference: [1] Journal of Organic Chemistry, 2007, vol. 72, # 8, p. 3122 - 3124
[2] Tetrahedron, 2010, vol. 66, # 13, p. 2474 - 2485
[3] Patent: US6355796, 2002, B1,
[4] Patent: US6140270, 2000, A,
[5] Patent: US5484763, 1996, A,
[6] Patent: EP908457, 1999, A1,
[7] Patent: US6191275, 2001, B1,
[8] Patent: EP1150962, 2004, B1, . Location in patent: Page 22
[9] Patent: US2002/28748, 2002, A1,
  • 5
  • [ 2142-68-9 ]
  • [ 23082-50-0 ]
Reference: [1] Journal of the American Chemical Society, 1915, vol. 37, p. 1262
[2] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 19, p. 5576 - 5581
  • 6
  • [ 25784-91-2 ]
  • [ 23082-50-0 ]
Reference: [1] Journal of the American Chemical Society, 1954, vol. 76, p. 5482
[2] Organic Process Research and Development, 2016, vol. 20, # 8, p. 1509 - 1519
  • 7
  • [ 2516-96-3 ]
  • [ 23082-50-0 ]
Reference: [1] Arzneimittel-Forschung/Drug Research, 1989, vol. 39, # 9, p. 1073 - 1080
[2] Organic Process Research and Development, 2016, vol. 20, # 8, p. 1509 - 1519
  • 8
  • [ 25784-91-2 ]
  • [ 35227-78-2 ]
  • [ 23082-50-0 ]
Reference: [1] Arzneimittel-Forschung/Drug Research, 1989, vol. 39, # 9, p. 1073 - 1080
  • 9
  • [ 25784-91-2 ]
  • [ 23082-50-0 ]
Reference: [1] Journal of Organic Chemistry, 1966, vol. 31, p. 677 - 681
  • 10
  • [ 2142-68-9 ]
  • [ 7697-37-2 ]
  • [ 23082-50-0 ]
Reference: [1] Journal of the American Chemical Society, 1915, vol. 37, p. 1262
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