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[ CAS No. 27465-51-6 ] {[proInfo.proName]}

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Chemical Structure| 27465-51-6
Chemical Structure| 27465-51-6
Structure of 27465-51-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 27465-51-6 ]

CAS No. :27465-51-6 MDL No. :MFCD00191646
Formula : C11H14O Boiling Point : -
Linear Structure Formula :- InChI Key :VGQRIILEZYZAOE-UHFFFAOYSA-N
M.W : 162.23 Pubchem ID :583750
Synonyms :

Calculated chemistry of [ 27465-51-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 3
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 51.22
TPSA : 17.07 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.4
Log Po/w (XLOGP3) : 2.99
Log Po/w (WLOGP) : 2.84
Log Po/w (MLOGP) : 2.69
Log Po/w (SILICOS-IT) : 3.34
Consensus Log Po/w : 2.85

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.9
Solubility : 0.204 mg/ml ; 0.00125 mol/l
Class : Soluble
Log S (Ali) : -3.01
Solubility : 0.158 mg/ml ; 0.000972 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.92
Solubility : 0.0195 mg/ml ; 0.000121 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 27465-51-6 ]

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

Application In Synthesis of [ 27465-51-6 ]

* 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.

  • Downstream synthetic route of [ 27465-51-6 ]

[ 27465-51-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 646-06-0 ]
  • [ 27465-51-6 ]
  • [ 6091-44-7 ]
  • [ 56839-43-1 ]
  • 2
  • [ 20024-90-2 ]
  • [ 2932-65-2 ]
  • [ 27465-51-6 ]
YieldReaction ConditionsOperation in experiment
With pyridine; N-hydroxyphthalimide; tetrabutylammonium tetrafluoroborate; oxygen; In 2,2,2-trifluoroethanol; acetonitrile; at 35℃;Electrolysis; General procedure: An undivided cell was equipped with a magnet stirrer, platinum plate electrode (1.0×1.0×0.3 cm3), as the working electrode and counter electrode. Substrate (0.5 mmol),nBu4NBF4 (0.5 mmol, 164.6 mg), N-hydroxyphthalimide (NHPI, 0.1 mmol, 16.3 mg), and pyridine (1.0 mmol, 82 μL)were added to MeCN/2,2,2-trifluoroethan-1-ol (TFE) (5:1,3 mL). The electrolysis was conducted in an undivided cell equipped with O2 balloon at a constant current of 5 mA at room temperature (25-30 C). When the reaction was completed, the solvent was removed under reduced pressure and the remaining crude product was purified by column chromatography over silica gel (petroleum ether/ethyl acetate(PE/EA)=30:1-10:1) to afford the corresponding aromatic ketone product.
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