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[ CAS No. 162504-75-8 ] {[proInfo.proName]}

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Chemical Structure| 162504-75-8
Chemical Structure| 162504-75-8
Structure of 162504-75-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 162504-75-8 ]

CAS No. :162504-75-8 MDL No. :MFCD02179013
Formula : C14H25NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :RWDYQFGCHAJYOJ-UHFFFAOYSA-N
M.W : 271.35 Pubchem ID :1502093
Synonyms :
Chemical Name :Methyl N-Boc-4-piperidinepropionate

Calculated chemistry of [ 162504-75-8 ]      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) : -6.51 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.37
Log Po/w (XLOGP3) : 2.04
Log Po/w (WLOGP) : 2.21
Log Po/w (MLOGP) : 1.85
Log Po/w (SILICOS-IT) : 1.82
Consensus Log Po/w : 2.26

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 : 1.22 mg/ml ; 0.00451 mol/l
Class : Soluble
Log S (Ali) : -2.84
Solubility : 0.392 mg/ml ; 0.00144 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 : 2.42

Safety of [ 162504-75-8 ]

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

Application In Synthesis of [ 162504-75-8 ]

* 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 [ 162504-75-8 ]

[ 162504-75-8 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 194933-85-2 ]
  • [ 162504-75-8 ]
  • 2
  • [ 162504-75-8 ]
  • [ 154775-43-6 ]
YieldReaction ConditionsOperation in experiment
A solution of tert-butyl 4- (3-METHOXY-3-OXOPROPYL) PIPERIDINE-1-CARBOXYLATE (2.0 g, 7.37 mmol) in 8 ml of methanol was added a solution of LIOH monohydrate (0.46g, 11.0 mmol) in 2 ml of water. The resulting solution was stirred at rt for 16h and it was concentrated under vacuum. To the residue was added 0.35 ml of acetic acid and 0.1 ml of water. The mixture was poured into a solution of EtOAc and CH2CL2 (1 : 1). The organic layer was dried with NA2SO4, filtered through celite and concentrated. To give 1.6g of 3- [1- (tert-butoxycarbonyl) piperidin-4- yl] propanoic acid.
  • 3
  • [ 498-94-2 ]
  • [ 162504-75-8 ]
  • 4
  • [ 24424-99-5 ]
  • [ 162504-75-8 ]
  • 5
  • [ 84358-13-4 ]
  • [ 162504-75-8 ]
  • 6
  • [ 139290-70-3 ]
  • [ 162504-75-8 ]
  • 7
  • [ 137076-22-3 ]
  • [ 162504-75-8 ]
  • 8
  • [ 162504-75-8 ]
  • C19H30N3O9P [ No CAS ]
  • 9
  • [ 162504-75-8 ]
  • [ 1027851-27-9 ]
  • 10
  • [ 162504-75-8 ]
  • 4-[2-([(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-methyl-propylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-ethyl]-piperidine-1-carboxylic acid tert-butyl ester [ No CAS ]
  • 11
  • [ 162504-75-8 ]
  • 3-(4-piperidinyl)propionyl-N-ethylglycyl-aspartyl-valine trifluoroacetate [ No CAS ]
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