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[ CAS No. 1211538-62-3 ]

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Chemical Structure| 1211538-62-3
Chemical Structure| 1211538-62-3
Structure of 1211538-62-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1211538-62-3 ]

CAS No. :1211538-62-3 MDL No. :MFCD14698134
Formula : C8H5BrF3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :284.03 g/mol Pubchem ID :46311228
Synonyms :

Calculated chemistry of of [ 1211538-62-3 ]

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 6.0
Num. H-bond donors : 0.0
Molar Refractivity : 48.22
TPSA : 39.19 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.26
Log Po/w (XLOGP3) : 2.65
Log Po/w (WLOGP) : 3.8
Log Po/w (MLOGP) : 2.11
Log Po/w (SILICOS-IT) : 2.96
Consensus Log Po/w : 2.75

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.37
Solubility : 0.122 mg/ml ; 0.000428 mol/l
Class : Soluble
Log S (Ali) : -3.12
Solubility : 0.213 mg/ml ; 0.000751 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.84
Solubility : 0.0414 mg/ml ; 0.000146 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.92

Safety of [ 1211538-62-3 ]

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 [ 1211538-62-3 ]

* 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 [ 1211538-62-3 ]

[ 1211538-62-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1211538-62-3 ]
  • [ 1227586-09-5 ]
YieldReaction ConditionsOperation in experiment
90% With methanol; sodium tetrahydroborate at 0 - 20℃; 10 To a solution of methyl 3-bromo-6-(trifluoromethyl)picolinate (B.6-1, 1 g, 3.53 mmol) in MeOH (50 ml) at 0 °C was added NaBH4(671 mg, 17.65 mmol). The reaction mixture was stirred at room temperature overnight, followed by concentration under reduced pressure. The resultant residue was dissolved in ethyl acetate (50 ml), washed with aq. NH4Cl (3 x 20 ml), dried over Na2SO4, filtered, and concentrated to afford the title compound. The residue was purified by column chromatography (eluted with 0-50% EtOAc/Hexane) to afford the title compound (B.6-2, 3.17 mmol, 806 mg, 90%) as a colorless liquid. LC-MS [M+H]+ = 255.95.
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