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[ CAS No. 53145-38-3 ] {[proInfo.proName]}

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Chemical Structure| 53145-38-3
Chemical Structure| 53145-38-3
Structure of 53145-38-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 53145-38-3 ]

CAS No. :53145-38-3 MDL No. :MFCD01631573
Formula : C7H6ClFO Boiling Point : No data available
Linear Structure Formula :- InChI Key :QASFEHCRPLPGES-UHFFFAOYSA-N
M.W : 160.57 Pubchem ID :2773581
Synonyms :

Calculated chemistry of [ 53145-38-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.9
TPSA : 9.23 ?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) : -5.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.17
Log Po/w (XLOGP3) : 2.61
Log Po/w (WLOGP) : 2.91
Log Po/w (MLOGP) : 2.84
Log Po/w (SILICOS-IT) : 2.88
Consensus Log Po/w : 2.68

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.86
Solubility : 0.223 mg/ml ; 0.00139 mol/l
Class : Soluble
Log S (Ali) : -2.45
Solubility : 0.565 mg/ml ; 0.00352 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.41
Solubility : 0.0626 mg/ml ; 0.00039 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.53

Safety of [ 53145-38-3 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H227-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 53145-38-3 ]

* 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 [ 53145-38-3 ]

[ 53145-38-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 53145-38-3 ]
  • [ 2040-90-6 ]
YieldReaction ConditionsOperation in experiment
With boron tribromide; In dichloromethane; at -78 - 20℃; for 16h; 2-Chloro-6-fluoro anisole (5 g, 31.13 mmol) was dissolved in DCM (300 mL) and cooled to about -78° C. To the solution was added BBr3 (7.35 mL, 77.8 mmol) in one portion. The reaction was warmed to r.t, stirred for about 16 hours and poured over ice to quench remaining BBr3. The material was partitioned between water and DCM (500 mL each). The aqueous layer was back extracted with DCM (200 mL), and the combined organics were dried (NaSO4), filtered and concentrated to give the product (4.60 g) as a dark oil. MS found 145.0 M-1
  • 2
  • [ 2040-90-6 ]
  • [ 74-88-4 ]
  • [ 53145-38-3 ]
YieldReaction ConditionsOperation in experiment
94% With potassium carbonate; In tetrahydrofuran; at 20℃; for 3h; Methyl iodide (850mul, 13.646mmol) and potassium carbonate (943mg, 6.824mmol) were added to <strong>[2040-90-6]2-chloro-6-fluorophenol</strong> (1.0g, 6.824mmol) in tetrahydrofuran (10ml) and the mixture was stirred at room temperature for 3 hours. The reaction mixture was partitioned between diethyl ether (50ml) and water (50ml). The organic phase was extracted and further washed with water (2 x 20ml) then dried over sodium sulphate and concentrated in vacuo to afford the title compound as a colourless liquid in 94percent yield, 1.03g.1HNMR(400MHz, CD3OD) delta: 3.90-3.91(s, 3H), 7.01-7.12(m, 2H), 7.18-7.21 (m, 1H)
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