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[ CAS No. 575-03-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 575-03-1
Chemical Structure| 575-03-1
Structure of 575-03-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 575-03-1 ]

CAS No. :575-03-1 MDL No. :MFCD00037578
Formula : C10H5F3O3 Boiling Point : -
Linear Structure Formula :- InChI Key :CCKWMCUOHJAVOL-UHFFFAOYSA-N
M.W : 230.14 Pubchem ID :5375667
Synonyms :
Chemical Name :7-Hydroxy-4-(trifluoromethyl)coumarin

Calculated chemistry of [ 575-03-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.1
Num. rotatable bonds : 1
Num. H-bond acceptors : 6.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.51
TPSA : 50.44 ?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) : -5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.58
Log Po/w (XLOGP3) : 2.42
Log Po/w (WLOGP) : 3.67
Log Po/w (MLOGP) : 2.04
Log Po/w (SILICOS-IT) : 2.93
Consensus Log Po/w : 2.53

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.19
Solubility : 0.149 mg/ml ; 0.000649 mol/l
Class : Soluble
Log S (Ali) : -3.12
Solubility : 0.174 mg/ml ; 0.000756 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.93
Solubility : 0.027 mg/ml ; 0.000117 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.58

Safety of [ 575-03-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 575-03-1 ]

* 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 [ 575-03-1 ]

[ 575-03-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 575-03-1 ]
  • [ 54109-16-9 ]
  • 7-(2-oxo-2-(2-(trifluoromethyl)phenyl)ethoxy)-4-(trifluoromethyl)-2H-chromen-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% With triethylamine; In tetrahydrofuran; at 20℃; for 24h; General procedure: The appropriate bromoketone (6a-o) (1.7 mmol) and triethylamine (1.6 mmol) were added to as olution of either7-hydroxy-4-methyl-2H-chromen-2-one 4 (1.4 mmol)or 7-hydroxy-4-(trifluoromethyl)-2H-chromen-2-one 5 (1.4 mmol) in THF (20 mL). The mixture was stirred at room temperature for 24h, filtered and the solvent was evaporated under reduced pressure.The solid residue was purified by column chromatography eluting with DCM/MeOH 9:1 to afford (7a-n) and (8a-o).
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