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[ CAS No. 1023-17-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1023-17-2
Chemical Structure| 1023-17-2
Structure of 1023-17-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1023-17-2 ]

CAS No. :1023-17-2 MDL No. :MFCD00017177
Formula : C15H14O2 Boiling Point : -
Linear Structure Formula :- InChI Key :PLALKSRAHVYFOH-UHFFFAOYSA-N
M.W : 226.27 Pubchem ID :231093
Synonyms :

Calculated chemistry of [ 1023-17-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.13
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 67.62
TPSA : 26.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.44 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.55
Log Po/w (XLOGP3) : 3.15
Log Po/w (WLOGP) : 3.12
Log Po/w (MLOGP) : 2.86
Log Po/w (SILICOS-IT) : 3.78
Consensus Log Po/w : 3.09

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.49
Solubility : 0.0739 mg/ml ; 0.000327 mol/l
Class : Soluble
Log S (Ali) : -3.37
Solubility : 0.096 mg/ml ; 0.000424 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.4
Solubility : 0.000895 mg/ml ; 0.00000395 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.55

Safety of [ 1023-17-2 ]

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 [ 1023-17-2 ]

* 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 [ 1023-17-2 ]

[ 1023-17-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 178686-24-3 ]
  • [ 1023-17-2 ]
  • [ 57-13-6 ]
  • [ 1283117-24-7 ]
YieldReaction ConditionsOperation in experiment
7.5% With hydrogenchloride; In ethanol; water; for 48.0h;Reflux; 165] To a mixture of l-(4-methoxyphenyl)-2-phenylethanone (200 mg, 0.88 mmol),<strong>[178686-24-3]3-ethoxy-4-hydroxy-5-nitrobenzaldehyde</strong> (187 mg, 0.89 mmol), and urea (159 mg, 2.65 mmol) in anhydrous EtOH (20 mL) was added concentrated HC1 solution (0.1 mL). The reaction mixture was refluxed for two days. When TLC (EtOAc:MeOH=10: l) showed that about 30% of the starting materials were consumed, the reaction mixture was concentrated. The residue was purified by column chromatography (EtOAc:MeOH=40: l) and preparative HPLC to afford Compound 20 as a yellow solid (30 mg, yield: 7.5%). 1H NMR (DMSO- 6 300 MHz): delta 10.30 (s, 1H), 8.65 (s, 1H), 7.52 (s, 1H), 7.45 (s, 1H), 7.20 (s, 1H), 7.09-7.15 (m, 2H), 6.96-7.08 (m, 3H), 6.75-6.82 (m, 4H), 5.12(s, 1H), 4.00-4.10 (m, 2H), 3.70 (s, 3H), 1.34(t, J = 6.9 Hz, 3H); MS (ESI): m/z 462.0 [M+l]+.
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