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[ CAS No. 135716-09-5 ] {[proInfo.proName]}

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Chemical Structure| 135716-09-5
Chemical Structure| 135716-09-5
Structure of 135716-09-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 135716-09-5 ]

CAS No. :135716-09-5 MDL No. :MFCD08275143
Formula : C14H25NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :PQEXLIRUMIRSAL-UHFFFAOYSA-N
M.W : 271.35 Pubchem ID :9993342
Synonyms :

Calculated chemistry of [ 135716-09-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 7
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 77.11
TPSA : 55.84 ?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) : -6.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.5
Log Po/w (XLOGP3) : 2.05
Log Po/w (WLOGP) : 2.21
Log Po/w (MLOGP) : 1.85
Log Po/w (SILICOS-IT) : 1.82
Consensus Log Po/w : 2.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.35
Solubility : 1.21 mg/ml ; 0.00445 mol/l
Class : Soluble
Log S (Ali) : -2.85
Solubility : 0.382 mg/ml ; 0.00141 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.16
Solubility : 1.88 mg/ml ; 0.00692 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.49

Safety of [ 135716-09-5 ]

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 [ 135716-09-5 ]

* 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 [ 135716-09-5 ]

[ 135716-09-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 135716-09-5 ]
  • [ 183170-69-6 ]
YieldReaction ConditionsOperation in experiment
With lithium borohydride; In methanol; diethyl ether; water; REFERENCE EXAMPLE 50 N-t-Butoxycarbonyl-4-(1-hydroxyethyl)piperidine In diethyl ether (20 ml) was dissolved ethyl N-tert-butoxycarbonyl-4-piperidineacetate (1.18 g) followed by addition of methanol (0.19 ml). Then, lithium borohydride (123 mg) was added under ice-cooling. The mixture was stirred at room temperature for 15 hours, after which time water was added under ice-cooling. The mixture was diluted with ethyl acetate, washed with aqueous NaCl solution, dried over MgSO4, and concentrated to provide the title compound as colorless oil (0.96 g). 1 H-NMR (CDCl3) δ: 1.0-1.4(4H,m), 1.45(9H,s), 1.5-1.8(4H,m), 2.69(2H,t,J=13.3Hz), 3.6-3.8(2H,brm), 4.0-4.2(2H,brm). IR (Neat): 3350, 2927, 1697, 1672, 1429, 1169 cm-1.
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