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[ CAS No. 4315-07-5 ] {[proInfo.proName]}

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Chemical Structure| 4315-07-5
Chemical Structure| 4315-07-5
Structure of 4315-07-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4315-07-5 ]

CAS No. :4315-07-5 MDL No. :MFCD00061239
Formula : C9H7F3O3 Boiling Point : -
Linear Structure Formula :- InChI Key :ZMTIBXQPXBUWPQ-UHFFFAOYSA-N
M.W : 220.15 Pubchem ID :2777319
Synonyms :

Calculated chemistry of [ 4315-07-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 4
Num. H-bond acceptors : 6.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.67
TPSA : 46.53 ?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) : -5.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.86
Log Po/w (XLOGP3) : 2.63
Log Po/w (WLOGP) : 3.47
Log Po/w (MLOGP) : 1.82
Log Po/w (SILICOS-IT) : 2.16
Consensus Log Po/w : 2.39

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.89
Solubility : 0.281 mg/ml ; 0.00128 mol/l
Class : Soluble
Log S (Ali) : -3.26
Solubility : 0.122 mg/ml ; 0.000553 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.81
Solubility : 0.341 mg/ml ; 0.00155 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.43

Safety of [ 4315-07-5 ]

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

Application In Synthesis of [ 4315-07-5 ]

* 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 [ 4315-07-5 ]
  • Downstream synthetic route of [ 4315-07-5 ]

[ 4315-07-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 64-17-5 ]
  • [ 4315-07-5 ]
  • [ 1206550-93-7 ]
YieldReaction ConditionsOperation in experiment
91% for 5 h; a) Sulfuric acid (0.484 ml, 9.08 mmol) was added dropwise to a solution of 2-(4-(trifluoromethoxy)phenyl)acetic acid (2.0 g, 9.08 mmol) in ethanol (20 ml), and heated under reflux for 5 hours. The reaction mixture was concentrated in vacuo, diluted with ethyl acetate (100 ml), washed with saturated NaHCO3 solution and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by column chromatography (ethyl acetate/hexane: 0/100 to 20/80) to give ethyl 2-(4-(trifluoromethoxy)phenyl)acetate (2.06 g, yield 91percent) as yellow oil.
Reference: [1] Patent: US2011/136833, 2011, A1, . Location in patent: Page/Page column 36
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