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[ CAS No. 95798-23-5 ] {[proInfo.proName]}

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Chemical Structure| 95798-23-5
Chemical Structure| 95798-23-5
Structure of 95798-23-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 95798-23-5 ]

CAS No. :95798-23-5 MDL No. :MFCD01863722
Formula : C13H17NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :JKIUUDJOCYHIGY-UHFFFAOYSA-N
M.W : 235.28 Pubchem ID :2794620
Synonyms :

Calculated chemistry of [ 95798-23-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.46
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 67.78
TPSA : 49.77 ?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) : -6.68 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.49
Log Po/w (XLOGP3) : 1.49
Log Po/w (WLOGP) : 1.25
Log Po/w (MLOGP) : 1.41
Log Po/w (SILICOS-IT) : 1.38
Consensus Log Po/w : 1.6

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.23
Solubility : 1.37 mg/ml ; 0.00583 mol/l
Class : Soluble
Log S (Ali) : -2.14
Solubility : 1.69 mg/ml ; 0.0072 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.42
Solubility : 0.901 mg/ml ; 0.00383 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.59

Safety of [ 95798-23-5 ]

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

Application In Synthesis of [ 95798-23-5 ]

* 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 [ 95798-23-5 ]

[ 95798-23-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5382-17-2 ]
  • [ 501-53-1 ]
  • [ 95798-23-5 ]
YieldReaction ConditionsOperation in experiment
76% With sodium hydroxide; In 1,4-dioxane; water; at 20℃; for 0.5h; Benzyl chloroformate (4.64 g, 27.199 mmol, 1.101 equiv) was added dropwise into a mixture of <strong>[5382-17-2]piperidin-4-ol hydrochloride</strong> (3.4 g, 24.71 mmol, 1.0 equiv), sodium hydroxide (2.17 g, 54.25 mmol, 2.2 equiv), and water (55 mL)/1 ,4-dioxane (55 mL). The resulting solution was stirred for 30 mm at room temperature. The mixture was diluted with water. The pH value of the mixture was adjusted to 2 with iN HC1. The resulting solution was extracted with ethyl acetate, washed with brine, dried over anhydrous sodium sulfate, and concentrated under vacuum. The residue was purified by a silica gel column eluting with ethyl acetate/petroleum ether (1:2). This resulted in the title compound (4.4 g, 76percent) as colorless oil.
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