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[ CAS No. 22237-13-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 22237-13-4
Chemical Structure| 22237-13-4
Structure of 22237-13-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 22237-13-4 ]

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Product Details of [ 22237-13-4 ]

CAS No. :22237-13-4 MDL No. :MFCD00674028
Formula : C8H11BO3 Boiling Point : -
Linear Structure Formula :(C2H5OC6H4)B(OH)2 InChI Key :WRQNDLDUNQMTCL-UHFFFAOYSA-N
M.W : 165.98 Pubchem ID :2734351
Synonyms :

Calculated chemistry of [ 22237-13-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 47.57
TPSA : 49.69 ?2

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) : -6.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.16
Log Po/w (WLOGP) : -0.23
Log Po/w (MLOGP) : 0.33
Log Po/w (SILICOS-IT) : -0.43
Consensus Log Po/w : 0.16

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.77
Solubility : 2.81 mg/ml ; 0.0169 mol/l
Class : Very soluble
Log S (Ali) : -1.8
Solubility : 2.64 mg/ml ; 0.0159 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.81
Solubility : 2.56 mg/ml ; 0.0154 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.69

Safety of [ 22237-13-4 ]

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 [ 22237-13-4 ]

* 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 [ 22237-13-4 ]

[ 22237-13-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 22237-13-4 ]
  • [ 55329-22-1 ]
  • rac-2-hydroxy-3,3-diphenyl-butyric acid cesium salt [ No CAS ]
  • 2-[4-(4-ethoxy-phenyl)-6-methyl-pyrimidin-2-yloxy]-3,3-diphenyl-butyric acid [ No CAS ]
  • 2
  • [ 22237-13-4 ]
  • [ 586-78-7 ]
  • [ 109662-72-8 ]
YieldReaction ConditionsOperation in experiment
91% With dichloro bis(acetonitrile) palladium(II); C95H120N20O10(10+)*10F6P(1-); potassium carbonate; In ethanol; at 50℃; for 1.5h; General procedure: In a typical run, a mixture of aryl bromide (0.50 mmol),phenylboronic acid (0.55 mmol), K2CO3 (1.5 mmol),0.2 mol% ligand, 1 mol% PdCl2(CH3CN)2 in 1.5 mL of ethanol were stirred at 50 C for 1.5 h under air. Solvent ethanol was removed completely under vacuum degree0.09 MPa at 45 C to give a crude product. The pure product was isolated by column chromatography on silica.
  • 3
  • [ 42872-74-2 ]
  • [ 22237-13-4 ]
  • 4'-ethoxy-6-methyl-biphenyl-3-carbonitrile [ No CAS ]
  • 4
  • [ 684284-68-2 ]
  • [ 22237-13-4 ]
  • [ 684287-25-0 ]
YieldReaction ConditionsOperation in experiment
21% With potassium carbonate;tetrakis(triphenylphosphine) palladium(0); In ethanol; water; toluene; at 120℃; for 6h; To a solution of trifluoro-methanesulfonic acid 9-benzhydryloxy-7-(4-fluoro- benzyl)-8-oxo-7,8-dihydro-6H-pyrrolo [3,4-g]quinolin-5-yl ester 46 (40 mg, 0.064 mmol) dissolved in toluene (3 mL)/ ethanol (0.6 mL)/ water (0.4 mL) was added K2C03 (27 mg, 0.192 mmol), 4-ethoxyphenolboronic acid (22 mg, 0.128 mmol) and tetrakis-(triphenylphosphine)-palladium(0) (15 mg, 0.013mmol). The reaction mixture in the flask was flashed with argon three times. It was then heated to 120C under argon 3 hours. The reaction was monitored by TLC (EtOAc/hexane 3/7) (Rf46 = 0.6, Rf275 = 0.4) and LC/MS. After cooling to room temperature, the mixture was diluted with EtOAc (20mL) and washed with IN HCl, saturated NaHC03 and brine. The organic phase was dried (MgS04), filtered and concentrated in vacuo. The residue was purified by silica gel chromatography ( ethylacetate/hexane - 1/3) to afford 9- benzhydryloxy-5-(4-ethoxy-phenyl)-7-(4-fluoro-benzyl)-6,7-dihydro-pyrrolo[3,4- g] quinolin-8-one 275 (8.0 mg, 21%) as a solid: 1H NMR (CDC13) No. 9.0 (d, 1H), 8.1 (s, 1H), 7.9 (d, 1H), 7.8-7.5 (dd, 4H), 7.5 (s, 1H), 7.4 (dd, 2H), 7.3-7.1 (m, 10H), 7.0 (t, 2H), 4.8 (s, 2H), 4.1 (m, 2H), 4.0 (s, 1H), 1.4 (t, 3H) ; MS: 595 (M+1).
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