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[ CAS No. 25137-01-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 25137-01-3
Chemical Structure| 25137-01-3
Structure of 25137-01-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 25137-01-3 ]

CAS No. :25137-01-3 MDL No. :MFCD03093637
Formula : C8H15NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :XIWBSOUNZWSFKU-SSDOTTSWSA-N
M.W : 157.21 Pubchem ID :185582
Synonyms :
Chemical Name :(R)-Ethyl piperidine-3-carboxylate

Calculated chemistry of [ 25137-01-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.46
TPSA : 38.33 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.2 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.21
Log Po/w (XLOGP3) : 0.08
Log Po/w (WLOGP) : 0.17
Log Po/w (MLOGP) : 0.69
Log Po/w (SILICOS-IT) : 1.22
Consensus Log Po/w : 0.87

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.67
Solubility : 33.8 mg/ml ; 0.215 mol/l
Class : Very soluble
Log S (Ali) : -0.44
Solubility : 57.2 mg/ml ; 0.364 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.56
Solubility : 4.36 mg/ml ; 0.0277 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.1

Safety of [ 25137-01-3 ]

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

Application In Synthesis of [ 25137-01-3 ]

* 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 [ 25137-01-3 ]

[ 25137-01-3 ] Synthesis Path-Downstream   1~4

  • 3
  • [ 25137-01-3 ]
  • [ 140645-24-5 ]
YieldReaction ConditionsOperation in experiment
Referential Example 3 (3S)-3-aminomethyl-1-(tert-butoxycarbonyl)piperidine The title compound was prepared by a method similar to Referential Example 1, using ethyl (3R)-3-piperidinecarboxylate L(+)-tartarate which was synthesiszed following the method of P. Magnus, et al. [J. Org. Chem., Vol. 56, pp. 1166-1170 (1991)].
  • 4
  • [ 25137-01-3 ]
  • [ 194726-40-4 ]
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