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[ CAS No. 175213-46-4 ] {[proInfo.proName]}

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Chemical Structure| 175213-46-4
Chemical Structure| 175213-46-4
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Product Details of [ 175213-46-4 ]

CAS No. :175213-46-4 MDL No. :MFCD01632529
Formula : C13H23NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ADFSCQGCEAKLOE-UHFFFAOYSA-N
M.W : 257.33 Pubchem ID :1514280
Synonyms :

Calculated chemistry of [ 175213-46-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.85
Num. rotatable bonds : 6
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 72.3
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) : -6.68 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.27
Log Po/w (XLOGP3) : 1.68
Log Po/w (WLOGP) : 1.82
Log Po/w (MLOGP) : 1.58
Log Po/w (SILICOS-IT) : 1.42
Consensus Log Po/w : 1.95

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.1
Solubility : 2.05 mg/ml ; 0.00798 mol/l
Class : Soluble
Log S (Ali) : -2.47
Solubility : 0.878 mg/ml ; 0.00341 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.76
Solubility : 4.48 mg/ml ; 0.0174 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.29

Safety of [ 175213-46-4 ]

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

Application In Synthesis of [ 175213-46-4 ]

* 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 [ 175213-46-4 ]

[ 175213-46-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 175213-46-4 ]
  • [ 183170-69-6 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; LiAlH4; In tetrahydrofuran; water; Step 3. 1-t-Butoxycarbonyl-4-(hydroxyethyl)piperidine To a solution of 5 g (696.6 mmol) of LiAlH4 in 800 mL of THF at rt was carefully added 30 g (232.2 mmol) of 1-t-butoxycarbonyl-4-(methoxycarbonyl methyl)piperidine and the reaction mixture was stirred at rt for 24 h. To the reaction mixture was slowly added 30 mL of H2O over a period of 2 h, followed by 30 mL of a 15% NaOH solution and 30 mL of H2O. The mixture was diluted with ether, filtered, and the solids were triturated several times with ethyl acetate. The combined organic fractions were concentrated to give the title compound.
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