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[ CAS No. 85803-62-9 ] {[proInfo.proName]}

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Chemical Structure| 85803-62-9
Chemical Structure| 85803-62-9
Structure of 85803-62-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 85803-62-9 ]

CAS No. :85803-62-9 MDL No. :MFCD01313808
Formula : C12H16N2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :GSRYZPWIWYYROI-UHFFFAOYSA-N
M.W : 204.27 Pubchem ID :2795566
Synonyms :

Calculated chemistry of [ 85803-62-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.42
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 68.09
TPSA : 23.55 ?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) : -6.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.19
Log Po/w (XLOGP3) : 1.32
Log Po/w (WLOGP) : 0.49
Log Po/w (MLOGP) : 1.04
Log Po/w (SILICOS-IT) : 1.68
Consensus Log Po/w : 1.34

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.1
Solubility : 1.61 mg/ml ; 0.00791 mol/l
Class : Soluble
Log S (Ali) : -1.42
Solubility : 7.85 mg/ml ; 0.0384 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.52
Solubility : 0.615 mg/ml ; 0.00301 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.57

Safety of [ 85803-62-9 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338-P310 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 85803-62-9 ]

* 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 [ 85803-62-9 ]

[ 85803-62-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19012-02-3 ]
  • [ 85803-62-9 ]
  • [ 1344706-49-5 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; In water; at 60℃; for 12h; General procedure: To a solution of N-methyl-3-acetylindol (1 mmol) and the benzaldehyde derivative (1 mmol) in methanol (10 ml) was added KOH (1 ml from a 50percent solution in H2O). The mixture was heated at 60 °C for 12 h then evaporated to dryness. The crude was dissolved in ethyl acetate (30 ml) then washed with HCl (1N, 10 ml) and H2O (10 ml), respectively. The organic layer was separated, dried over Na2SO4 and evaporated. The product was purified by chromatography column eluted with hexane:ethyl acetate (8:2) to yield the title compound as a yellow powder.
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