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[ CAS No. 1447953-13-0 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1447953-13-0
Chemical Structure| 1447953-13-0
Chemical Structure| 1447953-13-0
Structure of 1447953-13-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1447953-13-0 ]

CAS No. :1447953-13-0 MDL No. :MFCD25949184
Formula : C10H5BrF3N Boiling Point : -
Linear Structure Formula :- InChI Key :OEZOCEOAPZRERJ-UHFFFAOYSA-N
M.W : 276.05 Pubchem ID :18921566
Synonyms :

Calculated chemistry of [ 1447953-13-0 ]

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.1
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 54.45
TPSA : 12.89 Ų

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) : -5.21 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.39
Log Po/w (XLOGP3) : 3.91
Log Po/w (WLOGP) : 5.17
Log Po/w (MLOGP) : 3.53
Log Po/w (SILICOS-IT) : 4.07
Consensus Log Po/w : 3.81

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.44
Solubility : 0.00997 mg/ml ; 0.0000361 mol/l
Class : Moderately soluble
Log S (Ali) : -3.88
Solubility : 0.0364 mg/ml ; 0.000132 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.44
Solubility : 0.00101 mg/ml ; 0.00000365 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 1447953-13-0 ]

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 [ 1447953-13-0 ]

* 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 [ 1447953-13-0 ]

[ 1447953-13-0 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 325-13-3 ]
  • 3-bromo-6-trifluoromethyl-quinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine; bromine In tetrachloromethane 3.a a) a) 3-Bromo-6-trifluoromethyl-quinoline 19.7 g of 6-trifluoromethyl-quinoline is introduced into 200 ml of tetrachloromethane. 5.2 ml of bromine is instilled and the solution is refluxed for one hour. Within twenty minutes, 7.9 g of pyridine in 8 ml of tetrachloromethane is instilled in the boiling solution. After one hour, it is allowed to cool, decanted from the precipitated salt and the solution is concentrated by evaporation. After column chromatography, 14.6 g of 3-bromo-6-trifluoromethyl-quinoline of melting point 79° C. is obtained.
  • 2
  • [ 1447953-13-0 ]
  • [ CAS Unavailable ]
  • [ CAS Unavailable ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With triethylamine In toluene 3.b b) b) 6-Trifluoromethyl-quinoline-3-phosphonic acid diethyl ester 1.44 g of tetrakis-(triphenylphosphine)-palladium(O) are introduced in 16 ml of toluene, 3.8 ml of triethylamine and 3.6 ml of diethylphosphite at room temperature under nitrogen and mixed with 6.90 g of 3-bromo-6-trifluoromethyl-quinoline. It is stirred for two hours at 90° C. bath temperature. The mixture is diluted with ether, suctioned off and the filtrate is concentrated by evaporation. After column chromatography, 8.3 g of 6-trifluoromethyl-quinoline-3-phosphonic acid diethyl ester of melting point 69° C. is obtained.
  • 3
  • [ 1447953-13-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: triethylamine / toluene 2: acetic acid
  • 4
  • [ 1447953-13-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: triethylamine / toluene 2: acetic acid 3: tetrahydrofuran
  • 5
  • [ 1447953-13-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: triethylamine / toluene 2: acetic acid 3: tetrahydrofuran 4: nitronium tetrafluoroborate; sodium hydrogencarbonate / dichloromethane
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