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[ CAS No. 68301-99-5 ] {[proInfo.proName]}

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Chemical Structure| 68301-99-5
Chemical Structure| 68301-99-5
Structure of 68301-99-5 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Details of [ 68301-99-5 ]

CAS No. :68301-99-5 MDL No. :MFCD07367835
Formula : C18H18N2O4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :PFDJAEKKGJFCNL-UHFFFAOYSA-N
M.W : 326.35 Pubchem ID :12852091
Synonyms :

Calculated chemistry of [ 68301-99-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 24
Num. arom. heavy atoms : 14
Fraction Csp3 : 0.28
Num. rotatable bonds : 4
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 92.86
TPSA : 95.42 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.09
Log Po/w (XLOGP3) : 3.78
Log Po/w (WLOGP) : 3.23
Log Po/w (MLOGP) : 2.29
Log Po/w (SILICOS-IT) : 3.56
Consensus Log Po/w : 3.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.41
Solubility : 0.0126 mg/ml ; 0.0000387 mol/l
Class : Moderately soluble
Log S (Ali) : -5.48
Solubility : 0.00109 mg/ml ; 0.00000333 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.83
Solubility : 0.000477 mg/ml ; 0.00000146 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.16

Safety of [ 68301-99-5 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 68301-99-5 ]

* 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.

  • Upstream synthesis route of [ 68301-99-5 ]
  • Downstream synthetic route of [ 68301-99-5 ]

[ 68301-99-5 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 50743-32-3 ]
  • [ 105-56-6 ]
  • [ 68301-99-5 ]
Reference: [1] Journal of Medicinal Chemistry, 1985, vol. 28, # 5, p. 559 - 586
  • 2
  • [ 64-17-5 ]
  • [ 68301-99-5 ]
YieldReaction ConditionsOperation in experiment
13 mg for 1 h; Reflux Literature citation for methodology (Pfau et al., 2010). A suspension of 2 (15 mg, 0.05mmol) in EtOH (1 mL) was heated at reflux for 1 h. The mixture was concentrated to yield 3 (13mg, 84percent) as a light orange solid. 1H NMR (400 Mz, DMSO-d6) δ 8.80 (s, 1H), 8.36 (s, 1H), 8.09(s, 1H), 7.92 (d, J = 2.3 Hz, 1H), 7.74 (dd, J = 8.7, 2.3 Hz, 1H), 7.53 (d, J = 8.6 Hz, 1H), 4.35 (q, J = 7.1 Hz, 2H), 3.06 (p, J = 6.9 Hz, 1H), 1.36 (t, J = 7.1 Hz, 3H), 1.26 (d, J = 6.9 Hz, 6H). MSm/z 327.0 (M+H)+. HPLC 89percent.
Reference: [1] Molecular Pharmacology, 2018, vol. 94, # 4, p. 1210 - 1219
  • 3
  • [ 68302-57-8 ]
  • [ 68301-99-5 ]
Reference: [1] Molecular Pharmacology, 2018, vol. 94, # 4, p. 1210 - 1219
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