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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 : |
|
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 |
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 |
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 |
Lipinski : | 0.0 |
Ghose : | None |
Veber : | 0.0 |
Egan : | 0.0 |
Muegge : | 0.0 |
Bioavailability Score : | 0.55 |
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 |
PAINS : | 0.0 alert |
Brenk : | 0.0 alert |
Leadlikeness : | 0.0 |
Synthetic accessibility : | 1.92 |
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: |
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* 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.
Yield | Reaction Conditions | Operation 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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