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[ CAS No. 214360-60-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 214360-60-8
Chemical Structure| 214360-60-8
Structure of 214360-60-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 214360-60-8 ]

CAS No. :214360-60-8 MDL No. :MFCD02093722
Formula : C14H20BNO3 Boiling Point : No data available
Linear Structure Formula :CH3CONHC6H4B(OC(CH3)2C(CH3)2O) InChI Key :ANGKVUVZQVUVJO-UHFFFAOYSA-N
M.W : 261.12 Pubchem ID :2734619
Synonyms :

Calculated chemistry of [ 214360-60-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 77.23
TPSA : 47.56 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.42 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.08
Log Po/w (WLOGP) : 1.75
Log Po/w (MLOGP) : 1.13
Log Po/w (SILICOS-IT) : 1.46
Consensus Log Po/w : 1.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.81
Solubility : 0.409 mg/ml ; 0.00157 mol/l
Class : Soluble
Log S (Ali) : -2.71
Solubility : 0.511 mg/ml ; 0.00196 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.39
Solubility : 0.0107 mg/ml ; 0.000041 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.7

Safety of [ 214360-60-8 ]

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

Application In Synthesis of [ 214360-60-8 ]

* 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 [ 214360-60-8 ]

[ 214360-60-8 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 32578-30-6 ]
  • [ 25015-63-8 ]
  • [ 214360-60-8 ]
  • 2
  • [ 214360-60-8 ]
  • [ 500314-09-0 ]
  • 3-[10-(4-acetylamino-phenyl)-anthracen-9-yl]-5-methyl-isoxazole-4-carboxylic acid ethyl ester [ No CAS ]
  • 3
  • [ 214360-60-8 ]
  • [ 500314-10-3 ]
  • 3-[10-(4-acetylamino-phenyl)-anthracen-9-yl]-5-methyl-isoxazole-4-carboxylic acid ethyl ester [ No CAS ]
  • 4
  • [ 591-87-7 ]
  • [ 214360-60-8 ]
  • [ 104699-52-7 ]
  • 5
  • [ 21040-45-9 ]
  • [ 214360-60-8 ]
  • (E)-3-(4-acetamidophenyl)-1-phenylpropene [ No CAS ]
  • 6
  • [ 76644-52-5 ]
  • [ 214360-60-8 ]
  • <i>N</i>-(4-cyclohex-2-enyl-phenyl)-acetamide [ No CAS ]
  • 7
  • [ 533-58-4 ]
  • [ 214360-60-8 ]
  • [ 108779-65-3 ]
  • 8
  • [ 54245-42-0 ]
  • [ 214360-60-8 ]
  • C8(11)CH11NO [ No CAS ]
  • 9
  • [ 108-24-7 ]
  • [ 214360-73-3 ]
  • [ 214360-60-8 ]
YieldReaction ConditionsOperation in experiment
87% In dichloromethane; at 20℃; for 10h; To a mixture of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (3.0 g, 13.7 mmol) in DCM (70mL), was added acetic anhydride (7.0 g, 68.5 mmol). The reaction mixture was stirred at RT for 10 h. It was then concentrated under reduced pressure and the resulting residue was purified by flash column chromatography over silica gel (PE/EA 1:1, v/v) to give N-(4-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)phenyl) acetamide as a yellow solid (3.1 g, 87%). LC-MS (ESI): m/z (M+1)+ = 262.31.
  • 10
  • Pd(dppf)2Cl2 [ No CAS ]
  • [ 19524-06-2 ]
  • [ 214360-60-8 ]
  • [ 59656-60-9 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In tetrahydrofuran; Step 1: N-(4-(4-pyridyl)phenyl)acetamide A round bottom flask was charged with a 2 N Na2CO3 solution (4 equivalents) and THF and the mixture was sparged with N2 through a dispersion tube. 4-Bromopyridine hydrochloride (1 equivalent) and N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide (1.2 equivalents) were subsequently added, followed by Pd(dppf)2Cl2 (2.5 mol %). The reaction mixture was refluxed overnight, cooled to room temperature and diluted with EtOAc. The two phases were separated and the organic phase was washed with a 2 N Na2CO3 solution, brine, and dried (Na2SO4). Evaporation of the solvent under reduced pressure and purification by silica gel chromatography afforded the desired product as a white solid. MH+=213.1.
  • 11
  • [ 214360-60-8 ]
  • [ 333303-22-3 ]
  • ethyl 6-(4-acetamidophenyl)-7-(diethylamino)-2-oxo-2H-chromene-3-carboxylate [ No CAS ]
  • 12
  • [ 586-78-7 ]
  • [ 214360-60-8 ]
  • [ 28533-02-0 ]
  • 13
  • [ 104-92-7 ]
  • [ 214360-60-8 ]
  • [ 2221-22-9 ]
  • 14
  • [ 72601-11-7 ]
  • [ 214360-60-8 ]
  • N-[4-(2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl)phenyl]acetamide [ No CAS ]
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