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[ CAS No. 391668-75-0 ]

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Chemical Structure| 391668-75-0
Chemical Structure| 391668-75-0
Structure of 391668-75-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 391668-75-0 ]

CAS No. :391668-75-0 MDL No. :MFCD09878908
Formula : C14H17NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :CIZCOLAJWVBFIV-UHFFFAOYSA-N
M.W :247.29 g/mol Pubchem ID :17852149
Synonyms :

Calculated chemistry of [ 391668-75-0 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.43
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 72.76
TPSA : 46.61 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.27 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.6
Log Po/w (XLOGP3) : 2.17
Log Po/w (WLOGP) : 2.42
Log Po/w (MLOGP) : 1.86
Log Po/w (SILICOS-IT) : 2.38
Consensus Log Po/w : 2.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.72
Solubility : 0.468 mg/ml ; 0.00189 mol/l
Class : Soluble
Log S (Ali) : -2.78
Solubility : 0.409 mg/ml ; 0.00165 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.14
Solubility : 0.18 mg/ml ; 0.000726 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.38

Safety of [ 391668-75-0 ]

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 [ 391668-75-0 ]

* 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 [ 391668-75-0 ]
  • Downstream synthetic route of [ 391668-75-0 ]

[ 391668-75-0 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 214614-98-9 ]
  • [ 391668-75-0 ]
YieldReaction ConditionsOperation in experiment
86% With Dess-Martin periodane In dichloromethane at 20℃; for 0.5 h; The above product (163 mg, 0.654 mmol) was dissolved in 3.2 mL of dry dichloromethane, and Dess-Martin periodinane (290 mg, 0.68 mmol) was added to the solution at room temperature.
After the reaction mixture was stirred for 30 min at the same temperature, saturated NaHCO3 aqueous solution was added.
The mixture was extracted with ethyl acetate, and the extract was washed with brine, and dried over MgSO4.
After filtration, the filtrate was concentrated in vacuo and the residue was purified by silica gel column chromatography (hexane/ethyl acetate = 95/5 to 75/25) to obtain the title compound as a white powder (140 mg, 86percent).
Reference: [1] Patent: EP2123637, 2009, A1, . Location in patent: Page/Page column 80
[2] Patent: US2003/232860, 2003, A1, . Location in patent: Page 20
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