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[ CAS No. 130336-16-2 ] {[proInfo.proName]}

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Chemical Structure| 130336-16-2
Chemical Structure| 130336-16-2
Structure of 130336-16-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 130336-16-2 ]

CAS No. :130336-16-2 MDL No. :MFCD01319996
Formula : C8H3Cl2F3O Boiling Point : -
Linear Structure Formula :- InChI Key :DZDSQRPDUCSOQV-UHFFFAOYSA-N
M.W : 243.01 Pubchem ID :2758231
Synonyms :

Calculated chemistry of [ 130336-16-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.85
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 : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.05
Log Po/w (XLOGP3) : 3.98
Log Po/w (WLOGP) : 5.0
Log Po/w (MLOGP) : 3.37
Log Po/w (SILICOS-IT) : 4.03
Consensus Log Po/w : 3.69

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.04
Solubility : 0.0222 mg/ml ; 0.0000914 mol/l
Class : Moderately soluble
Log S (Ali) : -4.04
Solubility : 0.0222 mg/ml ; 0.0000913 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.47
Solubility : 0.00822 mg/ml ; 0.0000338 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.28

Safety of [ 130336-16-2 ]

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 [ 130336-16-2 ]

* 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 [ 130336-16-2 ]

[ 130336-16-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 46258-62-2 ]
  • [ 130336-16-2 ]
  • [ 1125724-14-2 ]
YieldReaction ConditionsOperation in experiment
40% Lithium diisopropylamide (Aldrich Chemical Company, 2M in tetrahydrofuran/ ethylbenzene, 4 mL, 7.94 mmol) was added to tetrahydrofuran (4 mL) at -78 0C. A solution of l-(4-bromo-l-naphthalenyl)ethanone (1.8 g, 7.22 mmol) in tetrahydrofuran (4 mL) was added dropwise to the mixture. When the addition was complete the mixture was stirred for 30 min at -78 0C. Then a solution of l-(3,5-dichlorophenyl)-2,2,2-trifluoroethanone (1.75 g, 7.20 mmol) in tetrahydrofuran (4 mL) was added dropwise to the mixture at such a rate that the temperature of the reaction mixture did not exceed -55 0C. The mixture was allowed to warm to ambient temperature over 120 min. The mixture was then poured into IN hydrochloric acid (100 mL) and extracted with ethyl acetate (2 x 100 mL). The combined extracts were dried and evaporated. Chromatography on silica gel (eluted with 1 :9 ethyl acetate/ hexanes) and crystallization from hexanes gave the title product as a white solid (1.1 g, 40% yield) melting at 74.5-75 0C (after recrystallization from hexanes). IR (nujol) 3409, 1684, 1569, 1505, 1407, 1343, 1232, 1170, 1141, 1121 cm-1.1H NMR (CDCl3) delta 8.38-8.30 (m, 2H), 7.90 (d, J=7.7 Hz, IH), 7.73-7.61 (m, 3H), 7.52 (s, 2H), 7.36 (t, J=I.8 Hz, IH), 5.86 (s, IH), 3.87 (1/2ABq, J=17.1 Hz, IH), 3.80 (1/2ABq, J=IlA Hz, IH).
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