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[ CAS No. 268218-94-6 ] {[proInfo.proName]}

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Chemical Structure| 268218-94-6
Chemical Structure| 268218-94-6
Structure of 268218-94-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 268218-94-6 ]

CAS No. :268218-94-6 MDL No. :MFCD05664212
Formula : C13H11BO3 Boiling Point : -
Linear Structure Formula :- InChI Key :CWMIVCCXDVRXST-UHFFFAOYSA-N
M.W : 226.04 Pubchem ID :4197235
Synonyms :

Calculated chemistry of [ 268218-94-6 ]

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 66.14
TPSA : 57.53 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.14 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.17
Log Po/w (WLOGP) : 0.6
Log Po/w (MLOGP) : 1.19
Log Po/w (SILICOS-IT) : 0.78
Consensus Log Po/w : 0.95

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.93
Solubility : 0.264 mg/ml ; 0.00117 mol/l
Class : Soluble
Log S (Ali) : -3.01
Solubility : 0.22 mg/ml ; 0.000975 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.76
Solubility : 0.0392 mg/ml ; 0.000173 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.89

Safety of [ 268218-94-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 268218-94-6 ]

* 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 [ 268218-94-6 ]

[ 268218-94-6 ] Synthesis Path-Downstream   1~2

  • 1
  • (4-benzoylphenyl)boronic acid [ No CAS ]
  • [ 27012-25-5 ]
  • [ 934564-29-1 ]
YieldReaction ConditionsOperation in experiment
17% With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In ethanol; N,N-dimethyl-formamide; for 7h;Heating / reflux; In a reaction container, 1.17 g (0.005 mol) of the compound (L-1), 1.41 g (0.00625 mol) of 4-benzoylphenylboric acid, 1.06 g (0.01 mol) of sodium carbonate, 0.35 g (0.0003 mol) of tetrakis(triphenylphosphine)palladium (0) were weighed and placed, and a dimethylformamide/ethanol solution mixture (35 mL/5 mL) was added. The reaction mixture was refluxed for 7 hours under nitrogen airflow. The reaction mixture was poured in water (100 mL) and extraction was performed with an ethyl acetate/hexane (1/1) solution (100 mL). Thereafter, the organic layer was washed with water (100 mL), a 5% aqueous sodium hydrogen carbonate solution (100 mL) and a saturated salt solution (100 mL). After the organic layer was dried over sodium sulfate, purification was performed by silica gel column chromatography (toluene/chloroform). The solvent was distilled off to obtain 0.28 g (0.00083 mol) of the compound (L-3) in a yield of 17%. LC-MS (positive) m/z:336 ([M+H]+) 1 H NMR (300MHz, CDC13) delta 7.46 (m, 1H),. delta 7.52 (dd, J = 7.5, 7.9 Hz, 4 H), delta 7.61 (m, 1 H), delta 7.77 (d, J = 8.3 Hz, 2 H), delta 7.85 (m, 3 H), delta 7.95 (d, J = 8.1 Hz, 2 H), delta 8.02 (dd, J = 2.4, 8.5 Hz, 1 H), delta 8.07 (m, 2 H), delta 9.00 (s, 1 H) .
  • 2
  • [ 268218-94-6 ]
  • [ 589-87-7 ]
  • [ 63242-14-8 ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate In N,N-dimethyl-formamide for 8h; Heating; Inert atmosphere; Synthesis of Raw Material Compound 1 4-Benzoylphenylboronic acid (2.7 g) (12 mmol) and 2.8 g of 1-bromo-4 iodobenzene (10 mmol) are dissolved in 50 ml of dimethyl formamide (DMF), and then 0.6 g of tetrakis(triphenylphosphine) platinum (0.5 mmol) and 6.5 g of cesium carbonate (20 mmol) are added thereto, and the reaction system is subjected to heating for 8 hour under nitrogen flow.After the reaction solution is allowed to be cooled, distilled water and about 600 ml of ethyl acetate are added and extraction is performed. After removing an aqueous layer and separating an organic layer, the system is dried with magnesium sulfate. The filtrate from which magnesium sulfate is filtered out is evaporated to dryness in a rotary evaporator, and refined by silica gel column (ethyl acetate/hexane: 1/10) to obtain 1.6 g of colorless raw material compound 1 (yield: 48%). The obtained compound 1 is confirmed to be an objective compound by mass spectrum and 1H NMR spectrum.
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