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[ CAS No. 98977-34-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 98977-34-5
Chemical Structure| 98977-34-5
Structure of 98977-34-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 98977-34-5 ]

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Product Details of [ 98977-34-5 ]

CAS No. :98977-34-5 MDL No. :MFCD01862189
Formula : C13H21NO5 Boiling Point : No data available
Linear Structure Formula :(CH3)3COCONC5H7OCO2CH2CH3 InChI Key :ABBVAMUCDQETDO-UHFFFAOYSA-N
M.W : 271.31 Pubchem ID :6420876
Synonyms :
Chemical Name :1-tert-Butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate

Calculated chemistry of [ 98977-34-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.77
Num. rotatable bonds : 6
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 72.5
TPSA : 72.91 ?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) : -7.21 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.74
Log Po/w (XLOGP3) : 1.05
Log Po/w (WLOGP) : 0.99
Log Po/w (MLOGP) : 0.67
Log Po/w (SILICOS-IT) : 1.15
Consensus Log Po/w : 1.32

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.79
Solubility : 4.42 mg/ml ; 0.0163 mol/l
Class : Very soluble
Log S (Ali) : -2.17
Solubility : 1.83 mg/ml ; 0.00673 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.64
Solubility : 6.16 mg/ml ; 0.0227 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.08

Safety of [ 98977-34-5 ]

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 [ 98977-34-5 ]

* 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 [ 98977-34-5 ]

[ 98977-34-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 57297-29-7 ]
  • [ 98977-34-5 ]
  • [ 1023953-54-9 ]
  • 2
  • [ 75-30-9 ]
  • [ 57297-29-7 ]
  • [ 98977-34-5 ]
  • [ 1318210-21-7 ]
YieldReaction ConditionsOperation in experiment
81% With potassium carbonate; In N,N-dimethyl-formamide; at 70℃; General procedure: A 10 mL round bottom flask was charged with phenylamidinium hydrochloride (31.7 mg, 0.203 mmol), 3-carbethoxy-4-piperidone hydrochloride (50 mg, 0.184 mmol), powdered K2CO3 (63.7 mg, 0.461 mmol), and a stirbar. The flask was sealed and charged with DMF (1.23 mL) followed by allyl chloride (37.9 muL, 0.461 mmol). With vigorous stirring, the reaction mixture was heated to 70 °C for 2 h, and reaction progress was monitored by LCMS. Upon completion of the reaction, the reaction mixture was diluted with EtOAc (10 mL), and washed with sat. aq NaHCO3 (10 mL) and brine (10 mL). The combined aqueous phases were back-extracted with EtOAc (5 mL), and the combined organic phases were dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residue was purified by gradient elution on silica gel (0-25percent EtOAc/hexanes) to afford the title compound.
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