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[ CAS No. 22446-38-4 ] {[proInfo.proName]}

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Chemical Structure| 22446-38-4
Chemical Structure| 22446-38-4
Structure of 22446-38-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 22446-38-4 ]

CAS No. :22446-38-4 MDL No. :MFCD07369387
Formula : C10H12O3 Boiling Point : -
Linear Structure Formula :- InChI Key :NSQBADKMIYCCSC-UHFFFAOYSA-N
M.W : 180.20 Pubchem ID :572437
Synonyms :

Calculated chemistry of [ 22446-38-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.14
TPSA : 46.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.95
Log Po/w (XLOGP3) : 1.54
Log Po/w (WLOGP) : 1.5
Log Po/w (MLOGP) : 1.67
Log Po/w (SILICOS-IT) : 1.91
Consensus Log Po/w : 1.71

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.0
Solubility : 1.78 mg/ml ; 0.00989 mol/l
Class : Soluble
Log S (Ali) : -2.13
Solubility : 1.35 mg/ml ; 0.00748 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.71
Solubility : 0.354 mg/ml ; 0.00196 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.6

Safety of [ 22446-38-4 ]

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

Application In Synthesis of [ 22446-38-4 ]

* 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 [ 22446-38-4 ]

[ 22446-38-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22446-38-4 ]
  • [ 146137-78-2 ]
  • [ 1198281-83-2 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In 1,4-dioxane; at 120℃; for 72h; Step 2: [3-(2-Forrayl-4-trifluoromethyl-phenoxy)-phenyl]-acetic acid ethyl ester; [00436] (3-Hydroxy-phenyl)-acetic acid ethyl ester (1.Og, 5.2mmol) 2-fluoro-5- (trifluoromethyl)benzaldehyde {0.72g, 5.2mmol), and potassium carbonate (1.44g, 10.4mmol) were combined in 1,4-dioxane (3OmL), and the reaction was stirred at 120C for 3 days. After work-up, the crude material was purified by silica gel chromatography (0-20% EtOAc in hexanes) to give the title compound.
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