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[ CAS No. 344329-76-6 ] {[proInfo.proName]}

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Chemical Structure| 344329-76-6
Chemical Structure| 344329-76-6
Structure of 344329-76-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 344329-76-6 ]

CAS No. :344329-76-6 MDL No. :MFCD08235066
Formula : C6H11NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :DGOYLVBDCVINQZ-UHFFFAOYSA-N
M.W : 129.16 Pubchem ID :13197203
Synonyms :

Calculated chemistry of [ 344329-76-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 32.83
TPSA : 52.32 ?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) : -7.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.07
Log Po/w (XLOGP3) : -0.55
Log Po/w (WLOGP) : -0.1
Log Po/w (MLOGP) : -0.41
Log Po/w (SILICOS-IT) : 0.54
Consensus Log Po/w : 0.11

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.23
Solubility : 76.4 mg/ml ; 0.591 mol/l
Class : Very soluble
Log S (Ali) : -0.08
Solubility : 108.0 mg/ml ; 0.833 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.33
Solubility : 60.6 mg/ml ; 0.469 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 344329-76-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 344329-76-6 ]

* 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 [ 344329-76-6 ]

[ 344329-76-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 344329-76-6 ]
  • [ 24424-99-5 ]
  • [ 301221-79-4 ]
  • tert-butyl 4-[2-(tetrahydro-2H-pyran-4-yl)-1,3-oxazol-4-yl]piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
Step A6.3-1: tert-Butyl 4-[2-(tetrahydro-2H-pyran-4-yl)-1,3-oxazol-4-yl]piperidine-1-carboxylatetert-Butyl 4-(bromoacetyl)piperidine-1-carboxylate (1.07 g, 3.49 mmol) and tetrahydro-2H-pyran-4-carboxamide (0.95 g, 7.36 mmol) were mixed heated in DMPU (6.99 mL) at 150° C. for 4 hrs. LC-MS indicated that the reaction was completed and the product showed loss of Boc group. Et3N (1.46 mL, 10.5 mol) and Boc2O (0.915 g, 4.19 mmol) were added and the mixture was stirred at RT for 30 min. The reaction was diluted with water and dichloromethane. The two layers were separated and the organic layer was extracted with dichloromethane. The combined organic layers were washed with H2O (twice) and brine, dried over Na2SO4, filtered and conc. The crude (still containing DMPU) was used without purification. LC-MS: [M+H]+=337.4.
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