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[ CAS No. 243128-37-2 ] {[proInfo.proName]}

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Chemical Structure| 243128-37-2
Chemical Structure| 243128-37-2
Structure of 243128-37-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 243128-37-2 ]

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Product Details of [ 243128-37-2 ]

CAS No. :243128-37-2 MDL No. :MFCD01569371
Formula : C8H6FNO Boiling Point : -
Linear Structure Formula :- InChI Key :FOWHAPVFVBXMBK-UHFFFAOYSA-N
M.W : 151.14 Pubchem ID :2737365
Synonyms :

Calculated chemistry of [ 243128-37-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.61
TPSA : 33.02 ?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) : -6.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.86
Log Po/w (XLOGP3) : 1.71
Log Po/w (WLOGP) : 2.13
Log Po/w (MLOGP) : 1.55
Log Po/w (SILICOS-IT) : 2.21
Consensus Log Po/w : 1.89

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.19
Solubility : 0.971 mg/ml ; 0.00643 mol/l
Class : Soluble
Log S (Ali) : -2.02
Solubility : 1.45 mg/ml ; 0.00957 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.87
Solubility : 0.203 mg/ml ; 0.00134 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.49

Safety of [ 243128-37-2 ]

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

Application In Synthesis of [ 243128-37-2 ]

* 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 [ 243128-37-2 ]

[ 243128-37-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 243128-37-2 ]
  • [ 508177-67-1 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogen; acetic acid;palladium 10% on activated carbon; under 3112.81 Torr; for 8h; Preparation 98; 4-Fluoro-3-methoxy-benz lamine; Add 4-fluoro-3-methoxy-benzonitrile (2 g, 0. 01 mol), 10% palladium on carbon (0.400 g) and glacial acetic acid (120 ml) to a pressure vessel. Purge the reaction vessel with nitrogen, purge the reaction vessel with hydrogen, pressurize the reaction mixture with hydrogen (415 Kpa), seal the vessel, and agitate the reaction. After 8 hours stop the agitation, vent the excess hydrogen from the vessel and purge the vessel with nitrogen. Filter the reaction mixture to remove the 5% palladium on carbon and return the filtrate for product isolation. Concentrate the crude solution, re-dissolve in CH2C12 (80mL) and washe with 5N NaOH (35mL). Separate the organic and aqueous phases and extract the aqueous with additional CHUCK (20mL). Combine the organic solutions, dry, filter and concentrate to give the crude material 2. 08g (100%). The title compound as the major product (Rf = 0.12, 10% MeOH/CH2C12) is used without further purification. MS (ES+) 156.1 (M+1) +. lH NMR (400MHz, CDC13) : 8 7. 01 (dd, 1H, J= 8.2, 11.4), 6.95 (dd, 1H, J = 2. 1,8. 4), 6.80 (m, 1H), 3.89 (s, 3H), 3.82 (s, 2H), 1.54 (br s, 2H).
86% A flame dried 50 mL round bottom flask was charged with lithium aluminum hydride (0.63 g, 16.6 mmol) and to this was added tetrahydrofuran (25 mL). The solution was cooled to 0 0C and 3-methoxy-4-fluorobenzonitrile (1.0 g, 6.62 mmol) was added in one portion. The ice bath was removed after an hour and the resulting mixture was stirred for 16 h after which it was cooled to 0 0C and quenched by adding 0.63 mL water, 0.63 mL 15% NaOH and 1.89 mL water drop- wise and in succession. The mixture was stirred for 20 min and filtered. The filtrate was concentrated in vacuo to obtain 890 mg (86%) of the title compound as an oil. NMR indicated no further purification was required. 1H NMR (300 MHz, DMSO-fife): δ 7.1 (m, 2H), 6.85 (m, IH), 3.84 (s, 3H), 3.7 (s, 2H). 13C NMR (75 MHz, DMSO-^6): δ 150.0 (d, J = 240 Hz), 146.6 (d, J = 10.5 Hz), 141.1 (d, J = 3.75 Hz), 118.75 (d, J = 6.75 Hz), 115.1 (d, J = 18 Hz), 112.5, 55.75, 45.2. HRMS: Calc'd for C8Hi0FNO (M + H): 156.0819; Found: 156.0818
  • 2
  • [ 56008-20-9 ]
  • [ 243128-37-2 ]
  • C19H20N2O2 [ No CAS ]
  • 3
  • [ 130723-13-6 ]
  • [ 243128-37-2 ]
  • 3-cyclopentyl-1-[(1R)-1-(4-fluoro-3-methoxyphenyl)-1-[3-fluoro-5-(trifluoromethyl)phenyl]-2-phenylethyl]urea [ No CAS ]
  • 4
  • [ 130723-13-6 ]
  • [ 243128-37-2 ]
  • benzylmagnesium halide [ No CAS ]
  • C22H18F5NO [ No CAS ]
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