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[ CAS No. 832114-05-3 ] {[proInfo.proName]}

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Chemical Structure| 832114-05-3
Chemical Structure| 832114-05-3
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Product Details of [ 832114-05-3 ]

CAS No. :832114-05-3 MDL No. :MFCD05863917
Formula : C18H28BNO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ANBFXKONRFZJAO-UHFFFAOYSA-N
M.W : 333.23 Pubchem ID :2760591
Synonyms :

Calculated chemistry of [ 832114-05-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 24
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.61
Num. rotatable bonds : 6
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 96.43
TPSA : 56.79 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.41
Log Po/w (WLOGP) : 2.86
Log Po/w (MLOGP) : 1.83
Log Po/w (SILICOS-IT) : 2.24
Consensus Log Po/w : 2.07

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.84
Solubility : 0.0478 mg/ml ; 0.000143 mol/l
Class : Soluble
Log S (Ali) : -4.28
Solubility : 0.0174 mg/ml ; 0.0000522 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.32
Solubility : 0.00158 mg/ml ; 0.00000474 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.35

Safety of [ 832114-05-3 ]

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

Application In Synthesis of [ 832114-05-3 ]

* 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 [ 832114-05-3 ]

[ 832114-05-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 73183-34-3 ]
  • [ 171663-13-1 ]
  • [ 832114-05-3 ]
YieldReaction ConditionsOperation in experiment
86.5% With potassium carbonate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; at 80℃; Bis(pinacolato) diboron (588mg, 2.0 mmol), reactant (286 mg, 1.0 mmol), potassium carbonate (276 mg, 2.0 mmol) and PdC12(dppf)CH2Cl2 (25 mg, 0.03 mmol) were added to a reaction flask which was purged thoroughly with N2. 10ml of dried dioxane was added via syringe and the reaction was heated to 80 0C for overnight. After LC-MS showed the reaction was complete, the solution was then cooled to room temperature and filtered and concentrated. Purification by chromatography (0-10% EtOAc: hexane), giving 288 mg of product as a white solid, yield: 86.5%. m/z 334 (M+H+).
83% With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate; In dimethyl sulfoxide; at 80℃; for 4h;Inert atmosphere; In the three-neck flask was added Intermediate j (10mmol),Pinacol diborate (2.67g, 10.5mmol),Potassium acetate (2.9g, 30mmol), [1,1'-bis(diphenylphosphine)ferrocene]palladium dichloromethane complex (245mg, 0.3mmol), protected by nitrogen, Add 15mL of dimethyl sulfoxide, and react at 80 C for 4 hours. Water was added after cooling, extraction with ethyl acetate, washing with saturated brine, and drying with anhydrous sodium sulfate. Column chromatography was used to obtain 2.76 g of intermediate k as a white solid
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