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[ CAS No. 1215-59-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1215-59-4
Chemical Structure| 1215-59-4
Structure of 1215-59-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1215-59-4 ]

CAS No. :1215-59-4 MDL No. :MFCD00005676
Formula : C15H13NO Boiling Point : No data available
Linear Structure Formula :C8H6NOCH2C6H5 InChI Key :JCQLPDZCNSVBMS-UHFFFAOYSA-N
M.W : 223.27 Pubchem ID :14624
Synonyms :

Calculated chemistry of [ 1215-59-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 15
Fraction Csp3 : 0.07
Num. rotatable bonds : 3
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 69.28
TPSA : 25.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.64 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.41
Log Po/w (XLOGP3) : 2.85
Log Po/w (WLOGP) : 3.6
Log Po/w (MLOGP) : 2.66
Log Po/w (SILICOS-IT) : 3.99
Consensus Log Po/w : 3.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.47
Solubility : 0.0748 mg/ml ; 0.000335 mol/l
Class : Soluble
Log S (Ali) : -3.03
Solubility : 0.206 mg/ml ; 0.000925 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.95
Solubility : 0.000249 mg/ml ; 0.00000111 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.66

Safety of [ 1215-59-4 ]

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

Application In Synthesis of [ 1215-59-4 ]

* 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 [ 1215-59-4 ]

[ 1215-59-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1215-59-4 ]
  • [ 878207-28-4 ]
  • [ 1309069-02-0 ]
YieldReaction ConditionsOperation in experiment
74.8% With caesium carbonate; In N,N-dimethyl-formamide; at 100℃;Inert atmosphere; Methyl 4-(5-(benzyloxy)-1H-indol-1-yl)-2-bromo-5-fluorobenzoate [0220] A mixture of 5-benzyloxy indole (11.2g, 0.05 mmol), methyl 2-bromo-4,5-difluoro-benzoate (12.6g, 0.05 mol) and Cs2C03 (24.4g, 0.075 mol) in DMF (150 mL) was stirred at 100 C under N2 atmosphere overnight. The mixture was cooled to room temperature and then filtrated. The filtrate was poured into 150 mL water. A gradual formation of a cream-colored precipitate was observed. Filtration gave the desired intermediate product as a cream-colored solid which is pure enough for further reaction (Yield: 17g, 74.8%). 1HNMR (500 MHz, DMSO-d6) delta: 8.02 (d, J=7 Hz, IH), 7.98 (d, J=l lHz, IH), 7.60 (s, IH), 7.48 (d, J=7.5 Hz, 2H), 7.39 (t, J=7.5 Hz, 2H), 7.32 (t, J=7 Hz, IH), 7.26 (d, J=8.5 Hz, 2H), 6.96 (d, J=8.5 Hz, IH), 6.68 (s, IH), 5.14 (s, 2H) and 3.91 (s, 3H) ppm.
  • 2
  • [ 1215-59-4 ]
  • [ 2150-46-1 ]
  • methyl 9-(benzyloxy)-2-hydroxy-6H-benzofuro[2,3-b]indole-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% With oxygen; copper(II) bis(trifluoromethanesulfonate); cobalt(II) chloride; In ethanol; at 40℃; under 760.051 Torr; for 48h;Sealed tube; Add 2-methyl carboxylate to phenol (0.2mmol, 1.0equiv.), 5-benzyloxyindole (0.2mmol, 1.0equiv.), CoCl2 (1.3mg, 5mol%) in a 25ml sample bottle, Cu(OTf)2 (7.3mg, 10mol%) and magnet, sealed with a rubber stopper, vacuumed and then filled with O2, transfer 4ml of 95% ethanol with a syringe to a sealed sample bottle, and then the atmosphere in the bottle Communicate with 1atm O2. After the reaction is stirred at 40 for 48h, the solvent is removed by blowing air at a constant temperature of 30 for 1 hour. The residue is purified by column chromatography on silica gel. The eluent is petroleum ether/ethyl acetate 20:1 To 5:1 gradient elution. The target product was collected and the isolated yield was 86%.
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