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[ CAS No. 849758-12-9 ] {[proInfo.proName]}

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Chemical Structure| 849758-12-9
Chemical Structure| 849758-12-9
Structure of 849758-12-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 849758-12-9 ]

CAS No. :849758-12-9 MDL No. :MFCD08436044
Formula : C8H6BrFO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :WDAFDKXHLVMFKA-UHFFFAOYSA-N
M.W : 233.03 Pubchem ID :21951878
Synonyms :

Calculated chemistry of [ 849758-12-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.38
TPSA : 26.3 ?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) : -5.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.34
Log Po/w (XLOGP3) : 2.57
Log Po/w (WLOGP) : 2.8
Log Po/w (MLOGP) : 3.09
Log Po/w (SILICOS-IT) : 2.79
Consensus Log Po/w : 2.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.14
Solubility : 0.168 mg/ml ; 0.000721 mol/l
Class : Soluble
Log S (Ali) : -2.77
Solubility : 0.395 mg/ml ; 0.0017 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.61
Solubility : 0.0569 mg/ml ; 0.000244 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.55

Safety of [ 849758-12-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 849758-12-9 ]

* 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 [ 849758-12-9 ]

[ 849758-12-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 849758-12-9 ]
  • [ 222978-01-0 ]
YieldReaction ConditionsOperation in experiment
92% With diisobutylaluminium hydride; In tetrahydrofuran; at 20℃; To a solution of 4-bromo-3-fluoro-benzoic acid methyl ester (5.3 g, 22.9 mmol) in dry THF (60 mL) was added diisobutylaluminum hydride (30 mL) dropwise, This mixture was stirred overnight at room temperature until the starting material had been consumed, quenched with saturated aqueous potassium tartrate solution and extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with brine, dried with Na2SO4, filtered, and evaporated to give white solid product (4.3 g, 92%).
A cooled (0 0C) suspension of lithium aluminum hydride (88 mg; 2.3 mmol) in anhydrous THF (10 mL) was treated dropwise with a solution of methyl 4-bromo-3-fluorobenzoate (Combi-Blocks; 300 mg; 1.29 mmol) dissolved in anhydrous Et2O (10 mL), and the reaction mixture was stirred at RT for 2 days. The reaction mixture was treated with a saturated aqueous solution of sodium thiosulfate. The organic phase was separated, dried over MgSO4, filtered and concentrated to dryness affording the title compound as a yellow liquid (247 mg, 94%). 1H NMR (300MHz, DMSO-d6) delta [ppm] 7.64 (1 H, dd, J= 8.1 , J= 7.5 Hz), 7.28 (1 H, m), 7.11 (1 H, m), 5.40 (1 H, t, J= 5.8 Hz), 4.48 (2H, d, J= 5.8 Hz). HPLC (Condition A): Rt 2.78 min (HPLC purity 90.2%).
  • 2
  • [ 849758-12-9 ]
  • [ 403-01-0 ]
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