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[ CAS No. 239482-98-5 ] {[proInfo.proName]}

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Chemical Structure| 239482-98-5
Chemical Structure| 239482-98-5
Structure of 239482-98-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 239482-98-5 ]

CAS No. :239482-98-5 MDL No. :MFCD01631187
Formula : C12H24N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QLEBCEWTHGUFFL-UHFFFAOYSA-N
M.W : 228.33 Pubchem ID :2756421
Synonyms :

Calculated chemistry of [ 239482-98-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.92
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 68.91
TPSA : 55.56 ?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) : -6.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.86
Log Po/w (XLOGP3) : 1.44
Log Po/w (WLOGP) : 1.74
Log Po/w (MLOGP) : 1.44
Log Po/w (SILICOS-IT) : 1.07
Consensus Log Po/w : 1.71

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.83
Solubility : 3.36 mg/ml ; 0.0147 mol/l
Class : Very soluble
Log S (Ali) : -2.21
Solubility : 1.4 mg/ml ; 0.00613 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.73
Solubility : 4.23 mg/ml ; 0.0185 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.84

Safety of [ 239482-98-5 ]

Signal Word:Danger Class:8
Precautionary Statements:P261-P280-P305+P351+P338 UN#:2735
Hazard Statements:H315-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 239482-98-5 ]

* 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 [ 239482-98-5 ]

[ 239482-98-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 239482-98-5 ]
  • [ 629655-23-8 ]
  • [ 629655-36-3 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In ethanol; for 72h;Heating / reflux; To a solution of tert-butyl 2-(2-aminoethyl)piperidine-1-carboxylate (1.50 g, 6.59 mmol) and <strong>[629655-23-8]2-chloro-3-nitropyridin-4-ol</strong> (0.959 g, 5.50 mmol) in 5 mL of EtOH, was added DIEA (1.50 mL, 8.25 mmol). The reaction was refluxed at 78 C. for 3 days, diluted with 200 mL of DCM, washed with 100 mL of saturated sodium bicarbonate solution (2×0 and concentrated. The residue was purified with 10% MeOH-DCM to give the title comnpound: 1H NMR (CDCl3) delta1.36-1.71 (m, 16H), 2.05-2.15 (b, 1H), 2.76-2.84 (t, 1H), 3.37 (b, 1H), 3.80 (b, 1H), 4.00 (b, 1H ), 4.39 (b, 1H), 6.24-6.25 (d, 1H, 5.5 Hz), 8.06-8.08 (d, 1H, 5.5 Hz), 12.4 (b, 1H). MS: MH+=367.
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