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[ CAS No. 406235-30-1 ] {[proInfo.proName]}

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Chemical Structure| 406235-30-1
Chemical Structure| 406235-30-1
Structure of 406235-30-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 406235-30-1 ]

CAS No. :406235-30-1 MDL No. :MFCD04972471
Formula : C11H21NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :SWUCHJAQBNXPBO-UHFFFAOYSA-N
M.W : 215.29 Pubchem ID :22730812
Synonyms :

Calculated chemistry of [ 406235-30-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.91
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.6
TPSA : 49.77 ?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) : -6.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.67
Log Po/w (XLOGP3) : 1.17
Log Po/w (WLOGP) : 1.39
Log Po/w (MLOGP) : 1.15
Log Po/w (SILICOS-IT) : 1.04
Consensus Log Po/w : 1.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.71
Solubility : 4.16 mg/ml ; 0.0193 mol/l
Class : Very soluble
Log S (Ali) : -1.81
Solubility : 3.33 mg/ml ; 0.0155 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.31
Solubility : 10.5 mg/ml ; 0.0488 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.21

Safety of [ 406235-30-1 ]

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

Application In Synthesis of [ 406235-30-1 ]

* 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 [ 406235-30-1 ]

[ 406235-30-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1120-95-2 ]
  • [ 406235-30-1 ]
  • tert-butyl 4-(pyridazin-3-yloxy)piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
Preparation of tert-butyl 4-(pyridazin-3-yloxy)piperidine-l-carboxylate. To a solution of tert-butyl 4-hydroxy-4-methylpiperidine-l-carboxylate (140 mg, 0.696 mmol) in DMF (2.3 mL) was added sodium hydride (60percent w/w, 56 mg, 1.39 mmol). The reaction was stirred for 10 min at ambient temperature. Then <strong>[1120-95-2]3-<strong>[1120-95-2]chloropyridazine</strong></strong> (159 mg, 1.39 mmol) was added and reaction stirred 3 h at 95°C. The reaction was cooled to ambient temperature and diluted with water and extracted with EtOAc. Combined organics were washed with saturated NaHC03(aq), water, and brine. The combined organic extracts were dried over anhydrous Na2S04(S), filtered and concentrated in vacuo to afford the title compound (assumed quantative yield, 194 mg) in sufficient purity for step 2. MS (apci) m/z = 280.2 (M+H).
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