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[ CAS No. 13222-85-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 13222-85-0
Chemical Structure| 13222-85-0
Structure of 13222-85-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 13222-85-0 ]

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Product Details of [ 13222-85-0 ]

CAS No. :13222-85-0 MDL No. :MFCD00048100
Formula : C16H14O3 Boiling Point : -
Linear Structure Formula :- InChI Key :BJMLLSSSTGHJJE-UHFFFAOYSA-N
M.W : 254.28 Pubchem ID :139413
Synonyms :

Calculated chemistry of [ 13222-85-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.12
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 72.56
TPSA : 43.37 ?2

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) : -5.73 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.57
Log Po/w (XLOGP3) : 2.99
Log Po/w (WLOGP) : 3.3
Log Po/w (MLOGP) : 4.04
Log Po/w (SILICOS-IT) : 3.82
Consensus Log Po/w : 3.34

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.5
Solubility : 0.0797 mg/ml ; 0.000314 mol/l
Class : Soluble
Log S (Ali) : -3.56
Solubility : 0.0693 mg/ml ; 0.000272 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.33
Solubility : 0.00119 mg/ml ; 0.00000467 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.83

Safety of [ 13222-85-0 ]

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

Application In Synthesis of [ 13222-85-0 ]

* 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 [ 13222-85-0 ]

[ 13222-85-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 13222-85-0 ]
  • [ 15980-22-0 ]
  • [ 321694-41-1 ]
  • 2
  • [ 13222-85-0 ]
  • [ 1765-93-1 ]
  • [ 530-46-1 ]
YieldReaction ConditionsOperation in experiment
80% With NHC-Pd(II)-Im; sodium hydrogencarbonate; In water; at 50℃; for 12h;Inert atmosphere; General procedure: Under N2 atmosphere, NaHCO3 (2.4 mmol), benzoic anhydride 3a (1.5 mmol), phenylboronic acid 2a (0.75 mmol), and H2O were successively added into a Schlenk reaction tube. The mixture was stirred at room temperature for about 10 min. Then NHC-Pd(II)-Im complex 1 (1.0 mol percent) was added. The mixture was stirred at room temperature for 12 h and then was diluted with CH2Cl2, washed with saturated brine, dried over anhydrous Na2SO4. The dried organic phase was then filtered, concentrated under reduced pressure and purified by flash column chromatography on silica gel to give the pure product 4a.
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