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[ CAS No. 154235-83-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
3d Animation Molecule Structure of 154235-83-3
Chemical Structure| 154235-83-3
Chemical Structure| 154235-83-3
Structure of 154235-83-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 154235-83-3 ]

CAS No. :154235-83-3 MDL No. :MFCD00943201
Formula : C14H15N3O Boiling Point : -
Linear Structure Formula :- InChI Key :ANDGGVOPIJEHOF-UHFFFAOYSA-N
M.W : 241.29 Pubchem ID :148184
Synonyms :
BDP 12;Ampalex;brand name: Ampalex.;Benzoyl-Piperidine-12;SPD 420;Ampakine CX 516
Chemical Name :Piperidin-1-yl(quinoxalin-6-yl)methanone

Calculated chemistry of [ 154235-83-3 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.36
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 73.66
TPSA : 46.09 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.22
Log Po/w (XLOGP3) : 1.89
Log Po/w (WLOGP) : 1.88
Log Po/w (MLOGP) : 1.46
Log Po/w (SILICOS-IT) : 2.35
Consensus Log Po/w : 1.96

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.81
Solubility : 0.377 mg/ml ; 0.00156 mol/l
Class : Soluble
Log S (Ali) : -2.48
Solubility : 0.798 mg/ml ; 0.00331 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.01
Solubility : 0.0237 mg/ml ; 0.0000982 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.66

Safety of [ 154235-83-3 ]

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

Application In Synthesis of [ 154235-83-3 ]

* 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 [ 154235-83-3 ]

[ 154235-83-3 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 453-71-4 ]
  • [ 154235-83-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 6 steps 1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 4 h / 20 °C 2: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 3 h / 100 °C 3: zinc; hydroxylamine hydrochloride / acetone; water / 3 h / Reflux 4: manganese(IV) oxide / dichloromethane / 4 h / 20 °C 5: triethylamine / dichloromethane / 5 h / 0 - 20 °C / Cooling with ice 6: 10% Pd/C; hydrogen / methanol
  • 2
  • [ CAS Unavailable ]
  • [ 154235-83-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 6 steps 1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 4 h / 20 °C 2: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 3 h / 100 °C 3: zinc; hydroxylamine hydrochloride / acetone; water / 3 h / Reflux 4: manganese(IV) oxide / dichloromethane / 4 h / 20 °C 5: triethylamine / dichloromethane / 5 h / 0 - 20 °C / Cooling with ice 6: 10% Pd/C; hydrogen / methanol
  • 3
  • [ 1096823-37-8 ]
  • [ 154235-83-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 5 steps 1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 3 h / 100 °C 2: zinc; hydroxylamine hydrochloride / acetone; water / 3 h / Reflux 3: manganese(IV) oxide / dichloromethane / 4 h / 20 °C 4: triethylamine / dichloromethane / 5 h / 0 - 20 °C / Cooling with ice 5: 10% Pd/C; hydrogen / methanol
  • 4
  • [ 2241677-03-0 ]
  • [ 154235-83-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: zinc; hydroxylamine hydrochloride / acetone; water / 3 h / Reflux 2: manganese(IV) oxide / dichloromethane / 4 h / 20 °C 3: triethylamine / dichloromethane / 5 h / 0 - 20 °C / Cooling with ice 4: 10% Pd/C; hydrogen / methanol
  • 5
  • [ 2241677-04-1 ]
  • [ 154235-83-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: manganese(IV) oxide / dichloromethane / 4 h / 20 °C 2: triethylamine / dichloromethane / 5 h / 0 - 20 °C / Cooling with ice 3: 10% Pd/C; hydrogen / methanol
  • 6
  • [ 2241677-05-2 ]
  • [ 154235-83-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: triethylamine / dichloromethane / 5 h / 0 - 20 °C / Cooling with ice 2: 10% Pd/C; hydrogen / methanol
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