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[ CAS No. 587886-11-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 587886-11-1
Chemical Structure| 587886-11-1
Structure of 587886-11-1 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 587886-11-1 ]

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Product Details of [ 587886-11-1 ]

CAS No. :587886-11-1 MDL No. :MFCD08458126
Formula : C11H5BrF3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :IMXGCAYXSYGXDF-UHFFFAOYSA-N
M.W : 320.06 Pubchem ID :11120770
Synonyms :

Calculated chemistry of [ 587886-11-1 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.09
Num. rotatable bonds : 2
Num. H-bond acceptors : 6.0
Num. H-bond donors : 1.0
Molar Refractivity : 61.4
TPSA : 50.19 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) : -5.89 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.86
Log Po/w (XLOGP3) : 3.33
Log Po/w (WLOGP) : 4.87
Log Po/w (MLOGP) : 1.88
Log Po/w (SILICOS-IT) : 3.5
Consensus Log Po/w : 3.09

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.85

Water Solubility

Log S (ESOL) : -4.2
Solubility : 0.0201 mg/ml ; 0.0000629 mol/l
Class : Moderately soluble
Log S (Ali) : -4.06
Solubility : 0.0278 mg/ml ; 0.0000869 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.79
Solubility : 0.00517 mg/ml ; 0.0000161 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.88

Safety of [ 587886-11-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 587886-11-1 ]

* 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 [ 587886-11-1 ]

[ 587886-11-1 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 124-38-9 ]
  • [ 18706-25-7 ]
  • [ 587886-11-1 ]
YieldReaction ConditionsOperation in experiment
88% With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -75℃; for 2h;
  • 2
  • [ 33513-42-7 ]
  • [ 587886-11-1 ]
  • 4-formyl-2-trifluoromethyl-3-quinolinecarboxylic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
56% Stage #1: 4-bromo-2-trifluoromethyl-3-quinolinecarboxylic acid With tetra(n-butyl)ammonium hydroxide In toluene Heating; Stage #2: N,N-dimethyl-formamide With n-butyllithium In tetrahydrofuran; hexane at -75℃; for 1h;
  • 3
  • [ 587886-11-1 ]
  • 2-trifluoromethyl-3-quinolinecarboxylic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
91% With n-butyllithium In diethyl ether; hexane at -75℃; for 6h;
67% With n-butyllithium In hexane at -75℃; for 6h;
Multi-step reaction with 3 steps 1: 95 percent / potassium carbonate / acetone / 6 h / 25 °C 2: 90 percent / tributyltin hydride; azoisobutyronitrile / tetrahydrofuran / 20 h / 75 °C 3: sodium hydroxide / H2O; methanol / 6 h / 50 °C
  • 4
  • [ 587886-11-1 ]
  • [ 74-88-4 ]
  • [ 587886-19-9 ]
YieldReaction ConditionsOperation in experiment
95% With potassium carbonate In acetone at 25℃; for 6h;
  • 5
  • [ 83842-55-1 ]
  • [ 587886-11-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 88 percent / phosphorus oxybromide / 2 h / 150 °C 2: 88 percent / butyllithium; diisopropylamine / tetrahydrofuran; hexane / 2 h / -75 °C
  • 6
  • [ 62-53-3 ]
  • [ 587886-11-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 51 percent / polyphosphoric acid / 2 h / 150 °C 2: 88 percent / phosphorus oxybromide / 2 h / 150 °C 3: 88 percent / butyllithium; diisopropylamine / tetrahydrofuran; hexane / 2 h / -75 °C
  • 7
  • [ 587886-11-1 ]
  • [ 587886-31-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 95 percent / potassium carbonate / acetone / 6 h / 25 °C 2: 90 percent / tributyltin hydride; azoisobutyronitrile / tetrahydrofuran / 20 h / 75 °C
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