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[ CAS No. 96551-22-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 96551-22-3
Chemical Structure| 96551-22-3
Structure of 96551-22-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 96551-22-3 ]

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Product Details of [ 96551-22-3 ]

CAS No. :96551-22-3 MDL No. :MFCD05864717
Formula : C14H17NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OOVPQKQFSDFRFA-UHFFFAOYSA-N
M.W : 247.29 Pubchem ID :11075767
Synonyms :

Calculated chemistry of [ 96551-22-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.36
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 70.27
TPSA : 51.46 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.77
Log Po/w (XLOGP3) : 2.38
Log Po/w (WLOGP) : 2.76
Log Po/w (MLOGP) : 2.04
Log Po/w (SILICOS-IT) : 1.96
Consensus Log Po/w : 2.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.98
Solubility : 0.26 mg/ml ; 0.00105 mol/l
Class : Soluble
Log S (Ali) : -3.1
Solubility : 0.196 mg/ml ; 0.000791 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.19
Solubility : 0.159 mg/ml ; 0.000641 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.27

Safety of [ 96551-22-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 96551-22-3 ]

* 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 [ 96551-22-3 ]

[ 96551-22-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 700-06-1 ]
  • [ 24424-99-5 ]
  • [ 96551-22-3 ]
YieldReaction ConditionsOperation in experiment
15% With dmap; triethylamine; In dichloromethane; at 20℃; for 1h; To a solution of <strong>[700-06-1]indole-3-carbinol</strong> (250 mg, 1.70 mmol) and (Boc)2O (371 mg, 1.70 mmol) in dichloromethane (6 mL) was added triethylamine (0.47 mL, 3.40 mmol) followed by DMAP (21 mg, 0.170 mmol). The reaction mixture was stirred at room temperature for 1 h and poured into water. The dichloromethane layer was separated, dried over Na2SO4 and concentrated. The crude product was purified by flash column chromatography on silica gel using 20%-30% EtOAc/hexanes as eluent to afford Boc protected indole as solid (60 mg, 0.243 mmol, 15%). 1H NMR (CDCl3, 300 MHz): delta (ppm) 1.66 (s, 9H), 1.84 (br s, 1H), 4.82 (s, 2H), 7.22-7.36 (m, 2H), 7.57 (s, 1H), 7.64 (dd, 1H, J=0.6, 7.5 Hz), 8.14 (d, 1H, J=8.1 Hz).
  • 2
  • [ 5683-31-8 ]
  • [ 96551-22-3 ]
  • C20H27NO4Si [ No CAS ]
  • 3
  • [ 700-06-1 ]
  • [ 96551-22-3 ]
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