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[ CAS No. 66171-50-4 ] {[proInfo.proName]}

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Chemical Structure| 66171-50-4
Chemical Structure| 66171-50-4
Structure of 66171-50-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 66171-50-4 ]

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Product Details of [ 66171-50-4 ]

CAS No. :66171-50-4 MDL No. :MFCD08436011
Formula : C7H7NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :JTVVPKLHKMKWNN-UHFFFAOYSA-N
M.W : 153.14 Pubchem ID :416343
Synonyms :

Calculated chemistry of [ 66171-50-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 37.54
TPSA : 59.42 ?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) : -6.75 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.56
Log Po/w (XLOGP3) : 0.68
Log Po/w (WLOGP) : 0.57
Log Po/w (MLOGP) : 0.15
Log Po/w (SILICOS-IT) : 0.71
Consensus Log Po/w : 0.74

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.49
Solubility : 4.96 mg/ml ; 0.0324 mol/l
Class : Very soluble
Log S (Ali) : -1.5
Solubility : 4.79 mg/ml ; 0.0313 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.51
Solubility : 4.73 mg/ml ; 0.0309 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.58

Safety of [ 66171-50-4 ]

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

Application In Synthesis of [ 66171-50-4 ]

* 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 [ 66171-50-4 ]

[ 66171-50-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 66171-50-4 ]
  • [ 109205-68-7 ]
YieldReaction ConditionsOperation in experiment
With LiAlH4; In tetrahydrofuran; ethanol; water; ethyl acetate; To a suspension of LiAlH4 (0.32 gm, 8.4 mmol) in 80 ml THF was added, slowly and dropwise, a solution of methyl 6-hydroxynicotinate (1.15 gm, 7.5 mmol) in 400 ml THF. The mixture was stirred at room temperature for 1.5 hours and then refluxed for 10 minutes. The mixture was then cooled and the reaction quenched with 3.0 ml of ethyl acetate and 1.5 ml of water. The solvents were removed and the residue was taken up in 40 ml of refluxing ethanol. The solution was filtered through celite and ethanol was evaporated in vacuo. The product was purified by silica gel chromatography using ethyl acetate/methanol (2:1) as the eluent. The product 5-hydroxymethyl-2-pyridone was crystallized from ethanol/ethyl acetate and the yield of the reaction was 0.65 gm (80%). HRMS: m/e, M+ found 125.0468, 100%. Calc. for C6H7NO2: 125.0477, -6 ppm. 1H NMR (d6-DMSO): 11.47 (broad, 1H, NH), 7.39 (dd, J3-4=9.5 Hz, J4-6=2.5 Hz, 1H, C(4) H), 7.23 (d, J4-6=2.5 Hz, 1H, C(6)H), 6.27 (d, J3-4=9.5 Hz, 1H, C(3)H), 5.10 (t, J=5.5 Hz, 1H, CH2OH), 4.17 (d, J=5.5 Hz, 2H, CH2OH). IR (cm-1): 3271 (m, broad), upsilon(O-H); 3124 (m, broad), upsilon(N-H); 3011(m), upsilon(C-H); 1661(vs), upsilon(C=O).
  • 2
  • [ 66171-50-4 ]
  • [ 109205-68-7 ]
YieldReaction ConditionsOperation in experiment
To a suspension of methyl 6-oxo-1 ,6-dihydro-3-pyridinecarboxylate (400 mg; Fluorochem) in THF (7 mL) was added dropwise 2M lithium borohydride in THF (6.53 mL) and the reaction mixture was heated at 55 0C under an atmosphere of argon for 5 hr. The reaction mixture was allowed to cool to RT and MeOH (4 mL) and water (1 mL) were added carefully. The mixture was stirred at room temperature for 20 min and then concentrated under reduced pressure. The crude product was purified by column chromatography, Biotage SP4, 25+M column, 0 - 30% MeOH / DCM. The fractions containing product were combined and concentrated under reduced pressure to give the title compound (68 mg) as a white solid, m/z [M+H]+: 125.9. Retention time 0.24 min (LC/MS method 3).
  • 3
  • [ 66171-50-4 ]
  • [ 77837-08-2 ]
  • 4
  • [ 66171-50-4 ]
  • [ 3719-45-7 ]
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