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[ CAS No. 120484-50-6 ] {[proInfo.proName]}

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Chemical Structure| 120484-50-6
Chemical Structure| 120484-50-6
Structure of 120484-50-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 120484-50-6 ]

CAS No. :120484-50-6 MDL No. :MFCD00671762
Formula : C9H9FO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :POHCKHGBDOTACV-UHFFFAOYSA-N
M.W : 168.17 Pubchem ID :2737355
Synonyms :

Calculated chemistry of [ 120484-50-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.09
TPSA : 26.3 ?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) : -6.13 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.86
Log Po/w (XLOGP3) : 1.68
Log Po/w (WLOGP) : 2.46
Log Po/w (MLOGP) : 1.86
Log Po/w (SILICOS-IT) : 2.58
Consensus Log Po/w : 2.09

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.18
Solubility : 1.11 mg/ml ; 0.00662 mol/l
Class : Soluble
Log S (Ali) : -1.85
Solubility : 2.39 mg/ml ; 0.0142 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.13
Solubility : 0.124 mg/ml ; 0.000736 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.41

Safety of [ 120484-50-6 ]

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

Application In Synthesis of [ 120484-50-6 ]

* 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 [ 120484-50-6 ]

[ 120484-50-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 94088-46-7 ]
  • [ 120484-50-6 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogenchloride; methyl magnesium iodide; In diethyl ether; Step A 2'-Fluoro-6'-methoxyacetophenone A mixture of <strong>[94088-46-7]2-fluoro-6-methoxybenzonitrile</strong> (15.94 g, 105.5 mmol) and a solution of methyl magnesium iodide in diethyl ether (3 M, 46.0 cm3, 137 mmol) was heated to 100 C. for 18 h. Upon cooling to room temperature, aqueous hydrochloric acid (3 M, 94 cm3) was added and the mixture was heated to reflux to for 4 h. When the reaction had cooled to room temperature the organic layer was separated and the aqueous phase was extracted with ethyl acetate (100 cm3). The combined organic extracts were washed with brine (100 cm3) before being dried (Na2SO4). The solvent was removed in vacuo to afford the title compound as an oil (117.7 g, 100%).
With methylmagnesium bromide; In benzene; Example 5 Preparation of 2-fluoro-6-methoxyacetophenone (5): To a flask containing methyl magnesium bromide (1.18 g, 9.93 mmol) in ether is added dropwise <strong>[94088-46-7]2-fluoro-6-methoxybenzonitrile</strong> (0.5 g, 3.31 mmol, Lancaster Synthesis Inc.) in benzene (9 ml). The reaction mixture is refluxed overnight. The reaction is cooled to room temperature and quenched slowly with saturated ammonium chloride (15 ml) and concentrated hydrochloric acid (1 ml). The mixture is extracted with diethyl ether (2*50 ml). The combined organic layers are dried over Na2 SO4, filtered, and rotary evaporated to give 0.55 g of a crude yellow material. Purification is accomplished by vacuum column (eluding with 16% ethyl acetate in hexane). The compoundcontaining fractions are combined, yielding 5.
  • 2
  • [ 75-16-1 ]
  • [ 94088-46-7 ]
  • [ 120484-50-6 ]
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