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[ CAS No. 312973-24-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 312973-24-3
Chemical Structure| 312973-24-3
Structure of 312973-24-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 312973-24-3 ]

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Product Details of [ 312973-24-3 ]

CAS No. :312973-24-3 MDL No. :MFCD00550641
Formula : C11H9NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :JVUPHJBFLSMOGY-UHFFFAOYSA-N
M.W : 203.19 Pubchem ID :762965
Synonyms :

Calculated chemistry of [ 312973-24-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.09
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 54.97
TPSA : 59.16 ?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) : -6.57 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.81
Log Po/w (XLOGP3) : 1.36
Log Po/w (WLOGP) : 1.77
Log Po/w (MLOGP) : 0.74
Log Po/w (SILICOS-IT) : 2.52
Consensus Log Po/w : 1.64

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.2
Solubility : 1.27 mg/ml ; 0.00627 mol/l
Class : Soluble
Log S (Ali) : -2.2
Solubility : 1.27 mg/ml ; 0.00624 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.31
Solubility : 0.0986 mg/ml ; 0.000485 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.49

Safety of [ 312973-24-3 ]

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

Application In Synthesis of [ 312973-24-3 ]

* 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 [ 312973-24-3 ]

[ 312973-24-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 93247-78-0 ]
  • [ 68-12-2 ]
  • [ 312973-24-3 ]
YieldReaction ConditionsOperation in experiment
93% To a stirred mixture of phosphorus oxychloride-dimethylformamide in anhydrous 1,2-dichloroethane (prepared by the slow addition of phosphorus oxychloride (0.43 ml, 4.6 mmol) to anhydrous DMF (0.35 ml, 4.6 mmol) in anhydrous 1,2-dichloroethane (6 ml) cooled below 5° C.) a solution of 7-methoxycarbonylindole (0.69 g, 4 mmol) in anhydrous 1,2-dichloroethane (6 ml) was dropwise below 5° C. The mixture was stirred at room temperature for 2 h and then was heated at 50° C. for 30 minutes. After cooling, the precipitate was filtered off and washed with 1,2-dichloroethane. This precipitate was suspended in aq Na2CO3 10percent (30 ml) and stirred at room temperature for 20 minutes; dichloromethane was added and stirring was continued 10 minutes more. The organic phase was separated and the aqueous phase was extracted with dichloromethane. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate and evaporated to yield 0.75 g (93percent) of the entitled product. Mp: 153-4° C.
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