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[ CAS No. 870837-18-6 ] {[proInfo.proName]}

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Chemical Structure| 870837-18-6
Chemical Structure| 870837-18-6
Structure of 870837-18-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 870837-18-6 ]

CAS No. :870837-18-6 MDL No. :MFCD09991722
Formula : C12H12N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :ZPKLQDKQGVSJST-UHFFFAOYSA-N
M.W : 216.24 Pubchem ID :27282445
Synonyms :

Calculated chemistry of [ 870837-18-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.17
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 60.41
TPSA : 44.12 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.01
Log Po/w (XLOGP3) : 1.51
Log Po/w (WLOGP) : 2.0
Log Po/w (MLOGP) : 0.66
Log Po/w (SILICOS-IT) : 2.12
Consensus Log Po/w : 1.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.44
Solubility : 0.78 mg/ml ; 0.00361 mol/l
Class : Soluble
Log S (Ali) : -2.04
Solubility : 1.95 mg/ml ; 0.00902 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.4
Solubility : 0.0865 mg/ml ; 0.0004 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.95

Safety of [ 870837-18-6 ]

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 [ 870837-18-6 ]

* 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 [ 870837-18-6 ]

[ 870837-18-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 288-32-4 ]
  • [ 870837-18-6 ]
  • [ 870837-70-0 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 130℃; Potassium carbonate (6.70 g) and imidazole (2.60 g) were added to a DMF (30 mL) solution of 4-fluoro-3-methoxybenzaldehyde (5.00 g) one by one, and the reaction solution was agitated at 130 C. overnight. After confirming disappearance of the starting materials, water and ethyl acetate were added to the reaction solution, and the organic layer was partitioned. After the obtained organic layer was washed with a saturated saline solution, it was dried over anhydrous magnesium sulfate and 4.76 g of crude aldehyde compounds was obtained by condensing under reduced pressure. The physical properties of the compound are as follows. 1H-NMR (CDCl3) delta (ppm): 10.01 (s, 1H), 7.92 (s, 1H), 7.57-7.60 (m, 2H), 7.49 (d, J=7.6 Hz, 1H), 7.29 (s, 1H), 7.21 (s, 1H), 3.98 (s, 3H).
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