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[ CAS No. 13391-27-0 ] {[proInfo.proName]}

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Chemical Structure| 13391-27-0
Chemical Structure| 13391-27-0
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Product Details of [ 13391-27-0 ]

CAS No. :13391-27-0 MDL No. :MFCD00619033
Formula : C10H10O2 Boiling Point : -
Linear Structure Formula :- InChI Key :IKUBQGOYKPKCKQ-UHFFFAOYSA-N
M.W : 162.19 Pubchem ID :4639349
Synonyms :

Calculated chemistry of [ 13391-27-0 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.67
TPSA : 22.37 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) : -5.37 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.45
Log Po/w (XLOGP3) : 2.7
Log Po/w (WLOGP) : 2.75
Log Po/w (MLOGP) : 1.53
Log Po/w (SILICOS-IT) : 2.84
Consensus Log Po/w : 2.46

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.04
Solubility : 0.149 mg/ml ; 0.000921 mol/l
Class : Soluble
Log S (Ali) : -2.82
Solubility : 0.244 mg/ml ; 0.0015 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.79
Solubility : 0.0262 mg/ml ; 0.000162 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.05

Safety of [ 13391-27-0 ]

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 [ 13391-27-0 ]

* 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 [ 13391-27-0 ]

[ 13391-27-0 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 584-82-7 ]
  • [ 13391-27-0 ]
Reference: [1] Journal of Organometallic Chemistry, 1998, vol. 560, # 1-2, p. 163 - 167
[2] Journal of Organic Chemistry, 2017, vol. 82, # 7, p. 3411 - 3424
[3] Zhurnal Obshchei Khimii, 1956, vol. 26, p. 2928,2930; engl. Ausg. S. 3255
[4] European Journal of Medicinal Chemistry, 2009, vol. 44, # 10, p. 3915 - 3921
  • 2
  • [ 918495-60-0 ]
  • [ 13391-27-0 ]
Reference: [1] Synthesis, 2006, # 20, p. 3419 - 3424
  • 3
  • [ 508168-22-7 ]
  • [ 13391-27-0 ]
Reference: [1] Synthesis, 2009, # 23, p. 3963 - 3966
  • 4
  • [ 121045-32-7 ]
  • [ 13391-27-0 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988, p. 3029 - 3036
  • 5
  • [ 17061-86-8 ]
  • [ 13391-27-0 ]
Reference: [1] Heterocycles, 1994, vol. 39, # 1, p. 371 - 380
  • 6
  • [ 82039-84-7 ]
  • [ 13391-27-0 ]
Reference: [1] Zhurnal Obshchei Khimii, 1956, vol. 26, p. 2928,2930; engl. Ausg. S. 3255
[2] Zhurnal Obshchei Khimii, 1957, vol. 27, p. 1090; engl. Ausg. S. 1174
  • 7
  • [ 29735-88-4 ]
  • [ 13391-27-0 ]
Reference: [1] Zhurnal Obshchei Khimii, 1956, vol. 26, p. 2928,2930; engl. Ausg. S. 3255
  • 8
  • [ 100117-70-2 ]
  • [ 13391-27-0 ]
Reference: [1] Zhurnal Obshchei Khimii, 1956, vol. 26, p. 2928,2930; engl. Ausg. S. 3255
  • 9
  • [ 7287-40-3 ]
  • [ 13391-27-0 ]
Reference: [1] Zhurnal Obshchei Khimii, 1956, vol. 26, p. 2928,2930; engl. Ausg. S. 3255
  • 10
  • [ 6769-56-8 ]
  • [ 77-78-1 ]
  • [ 13391-27-0 ]
Reference: [1] Zhurnal Obshchei Khimii, 1957, vol. 27, p. 1090; engl. Ausg. S. 1174
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