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[ CAS No. 189321-63-9 ] {[proInfo.proName]}

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Chemical Structure| 189321-63-9
Chemical Structure| 189321-63-9
Structure of 189321-63-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 189321-63-9 ]

CAS No. :189321-63-9 MDL No. :MFCD02179132
Formula : C12H21NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OKBNEDPOUYRYNP-UHFFFAOYSA-N
M.W : 243.30 Pubchem ID :23282848
Synonyms :

Calculated chemistry of [ 189321-63-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 67.72
TPSA : 66.84 ?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) : -6.73 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.39
Log Po/w (XLOGP3) : 1.49
Log Po/w (WLOGP) : 1.73
Log Po/w (MLOGP) : 1.31
Log Po/w (SILICOS-IT) : 0.99
Consensus Log Po/w : 1.58

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.02
Solubility : 2.31 mg/ml ; 0.00948 mol/l
Class : Soluble
Log S (Ali) : -2.5
Solubility : 0.768 mg/ml ; 0.00315 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.26
Solubility : 13.4 mg/ml ; 0.055 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.2

Safety of [ 189321-63-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 189321-63-9 ]

* 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 [ 189321-63-9 ]

[ 189321-63-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 189321-63-9 ]
  • [ 919354-20-4 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogenchloride; In 1,4-dioxane; at 20.0℃; for 2.0h; A. Preparation of 4-methylpiperidine 4-carboxylic acid. 1-(tert-Butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid (0.500 g, 2.06 mmol) was treated with 4 M HCl in dioxane (10 mL) for 2 hours at room temperature to afford the title compound (0.294 g, 100%) as the hydrochloride salt. MS (ES+) [M+H]+=144.0.
  • 2
  • [ 5369-19-7 ]
  • [ 189321-63-9 ]
  • [ 1192189-34-6 ]
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