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[ CAS No. 113209-68-0 ] {[proInfo.proName]}

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Chemical Structure| 113209-68-0
Chemical Structure| 113209-68-0
Structure of 113209-68-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 113209-68-0 ]

CAS No. :113209-68-0 MDL No. :MFCD06202344
Formula : C9H7FO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :HRPULQFHSZKTNA-UHFFFAOYSA-N
M.W : 166.15 Pubchem ID :14653132
Synonyms :

Calculated chemistry of [ 113209-68-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 40.97
TPSA : 26.3 ?2

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) : -6.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.86
Log Po/w (XLOGP3) : 1.48
Log Po/w (WLOGP) : 2.21
Log Po/w (MLOGP) : 1.47
Log Po/w (SILICOS-IT) : 2.83
Consensus Log Po/w : 1.97

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.17
Solubility : 1.12 mg/ml ; 0.00672 mol/l
Class : Soluble
Log S (Ali) : -1.64
Solubility : 3.81 mg/ml ; 0.0229 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.13
Solubility : 0.124 mg/ml ; 0.000745 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.95

Safety of [ 113209-68-0 ]

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

Application In Synthesis of [ 113209-68-0 ]

* 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.

  • Downstream synthetic route of [ 113209-68-0 ]

[ 113209-68-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 111141-00-5 ]
  • [ 113209-68-0 ]
  • [ 917248-49-8 ]
  • [ 1092938-99-2 ]
YieldReaction ConditionsOperation in experiment
With sodium tetrahydroborate; In methanol; at 0 - 20℃; for 18h; At a temperature of 0 0C, sodium borohydride (7.4 g, 195 mmol) was added portion-wise to a mixture of 7-fluoro-2,3-dihydro-4/-/-chromen-4-one and 8-fluoro-2,3-dihydro-4/-/-chromen-4-one (16.2 g, 97.5 mmol) in methanol (200 ml). After a period of 1 hour at 0 0C and 17 hours at room temperature, the reaction mixture was quenched with saturated ammonium chloride solution (400 ml) and water (200 ml), and extracted with dichloromethane (2 x). The combined organic phases were washed with water and saturated sodium chloride solution, dried over magnesium sulfate, and the solvent was evaporated. The yellow residue crystallized slowly. The title compound was isolated as mixture with 8- fluorochroman-4-ol (16.28 g, 99 % yield).
  • 2
  • [ 133077-42-6 ]
  • [ 111141-00-5 ]
  • [ 113209-68-0 ]
YieldReaction ConditionsOperation in experiment
A solution of 3-(3-fluorophenoxy)propanoic acid (20.0 g, 108 mmol) in toluene (230 ml) and thionyl chloride (64.3 g, 0.54 mol) was refluxed for 17 hours. The reaction mixture was concentrated several times in the presence of toluene. A solution of the yellow oily residue in chloroform (200 ml) was cooled to -65 0C and treated with trifluoromethanesulfonic acid (48.0 ml, 0.54 mol, addition over 45 min). The brown solution was gradually warmed to room temperature. After a period of 17 h, the reaction mixture was poured on ice water (1 I) and the phases were separated. The aqueous phase was extracted with chloroform (200 ml). The combined organic phases were washed with 1 N sodium hydroxide solution (2 x 200 ml), water, and saturated sodium chloride solution, and dried over magnei- sum sulfate. Evaporation of the solvent afforded the title compound as mixture with 8-fluoro-2,3- dihydro-4/-/-chromen-4-one (16.26 g of a yellow solid, 91 % yield).
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