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[ CAS No. 386704-06-9 ] {[proInfo.proName]}

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Chemical Structure| 386704-06-9
Chemical Structure| 386704-06-9
Structure of 386704-06-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 386704-06-9 ]

CAS No. :386704-06-9 MDL No. :MFCD01862660
Formula : C7H2ClF3N2 Boiling Point : -
Linear Structure Formula :- InChI Key :CDSFASYGONAHHN-UHFFFAOYSA-N
M.W : 206.55 Pubchem ID :2778413
Synonyms :

Calculated chemistry of [ 386704-06-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.96
TPSA : 36.68 ?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) : -5.82 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 2.45
Log Po/w (WLOGP) : 3.78
Log Po/w (MLOGP) : 1.47
Log Po/w (SILICOS-IT) : 2.99
Consensus Log Po/w : 2.47

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.94
Solubility : 0.237 mg/ml ; 0.00115 mol/l
Class : Soluble
Log S (Ali) : -2.86
Solubility : 0.283 mg/ml ; 0.00137 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.62
Solubility : 0.0495 mg/ml ; 0.00024 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.89

Safety of [ 386704-06-9 ]

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

Application In Synthesis of [ 386704-06-9 ]

* 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 [ 386704-06-9 ]

[ 386704-06-9 ] Synthesis Path-Downstream   1~5

  • 2
  • [ 386704-06-9 ]
  • [ 108-82-7 ]
  • [ 935519-04-3 ]
YieldReaction ConditionsOperation in experiment
With 1,8-diazabicyclo[5.4.0]undec-7-ene; at 50℃; General procedure: To a stirred solution of 4 (1.0 mmol) in 1,4-dioxane or acetonitrile (5 mL) at 0 C was added 1,8-diazabicyclo[5.4.0]undec-7-ene (2 mmol) followed by alcohol compound (1.2 mmol). The reaction mixture was stirred at 50 C for overnight, and extracted with EtOAc for several times. The combined organic layers were washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexane (1:2) as eluant.
  • 3
  • [ 386704-06-9 ]
  • [ 108-82-7 ]
  • [ 1444005-86-0 ]
  • 4
  • [ 386704-06-9 ]
  • [ 60211-57-6 ]
  • C14H7Cl2F3N2O [ No CAS ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In N,N-dimethyl-formamide; at 60 - 90℃; General procedure: To a stirred solution of 4 (1.0 mmol) in N,N-dimethylformamide (5 mL) at 0 C was added cesium carbonate (3.0 mmol) followed by alcohol compound (1.2 mmol). The reaction mixture was stirred at 60-90 C for overnight, and extracted with EtOAc several times. The combined organic layers were washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexane (1:2) as eluant.
  • 5
  • [ 386704-06-9 ]
  • [ 60211-57-6 ]
  • [ 1444006-01-2 ]
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; ;