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[ CAS No. 864685-26-7 ] {[proInfo.proName]}

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Chemical Structure| 864685-26-7
Chemical Structure| 864685-26-7
Structure of 864685-26-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 864685-26-7 ]

CAS No. :864685-26-7 MDL No. :MFCD05864767
Formula : C14H13IN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :GADLXNFRAAUWAD-UHFFFAOYSA-N
M.W : 368.17 Pubchem ID :17749979
Synonyms :

Calculated chemistry of [ 864685-26-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.29
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 81.57
TPSA : 55.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.19
Log Po/w (XLOGP3) : 3.64
Log Po/w (WLOGP) : 3.9
Log Po/w (MLOGP) : 2.74
Log Po/w (SILICOS-IT) : 3.07
Consensus Log Po/w : 3.31

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.57
Solubility : 0.00995 mg/ml ; 0.000027 mol/l
Class : Moderately soluble
Log S (Ali) : -4.48
Solubility : 0.0121 mg/ml ; 0.0000328 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.34
Solubility : 0.0168 mg/ml ; 0.0000456 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.74

Safety of [ 864685-26-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H312-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 864685-26-7 ]

* 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 [ 864685-26-7 ]

[ 864685-26-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1092114-59-4 ]
  • [ 24424-99-5 ]
  • [ 864685-26-7 ]
YieldReaction ConditionsOperation in experiment
100% With dmap; triethylamine; In dichloromethane; at 20.0℃; for 0.666667h; 5-Cyano-3-iodoindole (0.700 g, 2.61 mmol) obtained in Step 1 was dissolved in dichloromethane (40 mL), and the mixture was stirred at room temperature for 40 minutes after adding di-tert-butyl dicarbonate (0.627 g, 2.87 mmol), triethylamine (1.09 mL, 7.83 mmol), and 4-dimethylaminopyridine (32.0 mg, 0.261 mmol). The mixture was diluted with ethyl acetate, and washed with 1 mol/L hydrochloric acid and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give 1-tert-butoxycarbonyl-5-cyano-3-iodoindolo (0.958 g, quantitative). ESI-MS: m/z 369 [M + H]+.
  • 2
  • [ 864685-26-7 ]
  • tert-butyl 5-cyano-3-hydroxy-1H-indole-1-carboxylate [ No CAS ]
  • 3
  • [ 864685-26-7 ]
  • 1,3-dioxoisoindolin-2-yl tetrahydro-2H-pyran-4-carboxylate [ No CAS ]
  • tert-butyl 5-cyano-3-(tetrahydro-2H-pyran-4-yl)-1H-indole-1-carboxylate [ No CAS ]
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