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[ CAS No. 914223-43-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 914223-43-1
Chemical Structure| 914223-43-1
Structure of 914223-43-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 914223-43-1 ]

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Product Details of [ 914223-43-1 ]

CAS No. :914223-43-1 MDL No. :MFCD06797827
Formula : C7H6FNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :WZCZMWMNVHEBCK-UHFFFAOYSA-N
M.W : 155.13 Pubchem ID :23094343
Synonyms :

Calculated chemistry of [ 914223-43-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 37.76
TPSA : 63.32 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.87
Log Po/w (XLOGP3) : 0.87
Log Po/w (WLOGP) : 1.53
Log Po/w (MLOGP) : 0.32
Log Po/w (SILICOS-IT) : 0.92
Consensus Log Po/w : 0.9

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.69
Solubility : 3.19 mg/ml ; 0.0205 mol/l
Class : Very soluble
Log S (Ali) : -1.78
Solubility : 2.55 mg/ml ; 0.0165 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.68
Solubility : 3.27 mg/ml ; 0.0211 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.12

Safety of [ 914223-43-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 914223-43-1 ]

* 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 [ 914223-43-1 ]

[ 914223-43-1 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 317-46-4 ]
  • [ 914223-43-1 ]
Reference: [1] RSC Advances, 2019, vol. 9, # 15, p. 8389 - 8393
[2] Patent: US2009/286783, 2009, A1, . Location in patent: Page/Page column 57-58
[3] Patent: US2009/306087, 2009, A1, . Location in patent: Page/Page column 44-45
[4] Patent: WO2011/63159, 2011, A1, . Location in patent: Page/Page column 197
[5] European Journal of Medicinal Chemistry, 2013, vol. 66, p. 450 - 465
  • 2
  • [ 914223-43-1 ]
  • [ 1195768-19-4 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 15, p. 4436 - 4440
[2] Patent: WO2018/55097, 2018, A1,
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