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[ CAS No. 20826-94-2 ] {[proInfo.proName]}

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Chemical Structure| 20826-94-2
Chemical Structure| 20826-94-2
Structure of 20826-94-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 20826-94-2 ]

CAS No. :20826-94-2 MDL No. :MFCD00044715
Formula : C9H14O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :PJMKFKUFBDXYEC-UHFFFAOYSA-N
M.W : 170.21 Pubchem ID :2723663
Synonyms :

Calculated chemistry of [ 20826-94-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.78
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.75
TPSA : 43.37 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.19
Log Po/w (XLOGP3) : 0.62
Log Po/w (WLOGP) : 1.31
Log Po/w (MLOGP) : 0.9
Log Po/w (SILICOS-IT) : 1.89
Consensus Log Po/w : 1.38

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.02
Solubility : 16.2 mg/ml ; 0.0951 mol/l
Class : Very soluble
Log S (Ali) : -1.11
Solubility : 13.4 mg/ml ; 0.0785 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.81
Solubility : 2.65 mg/ml ; 0.0156 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.43

Safety of [ 20826-94-2 ]

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

Application In Synthesis of [ 20826-94-2 ]

* 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 [ 20826-94-2 ]

[ 20826-94-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 20826-94-2 ]
  • [ 78603-91-5 ]
  • (4S,8R,11S)-(-)-11-Methyl-10,10-diphenyl-9-oxa-1-azatricyclo[6.3.0.04,8]undecan-2-one [ No CAS ]
  • 2
  • [ 20826-94-2 ]
  • [ 14150-94-8 ]
  • [ 904929-05-1 ]
YieldReaction ConditionsOperation in experiment
With ammonia; In methanol;Heating / reflux; Intermediate 5-1A mixture of l-methyl-3, 5-dinitro-2-pyridone (11.7 g, 59 mmol) and ethyl cyclopentanoneacetate (10 g, 59 mmol) in 2 M NH3MeOH (300 niL) was refluxed overnight and then cooled to room temperature. Methanol was removed in vacuo and the residue was partitioned between EtOAc (200 mL) and water (400 mL). The aqueous layer was further extracted with EtOAc (2 x 150 mL). The organic layers were combined, washed with brine (150 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (eluting with a gradient of 0 to 20% EtOAc/hexanes) to give pure product as light yellow oil. LC-MS for C12H15N2O4 [M+H+] : calculated 251.1, found 251.2. EPO <DP n="22"/>
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