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[ CAS No. 319-24-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 319-24-4
Chemical Structure| 319-24-4
Structure of 319-24-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 319-24-4 ]

CAS No. :319-24-4 MDL No. :MFCD03791308
Formula : C8H8FNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :PUDDYSBKCDKATP-UHFFFAOYSA-N
M.W : 169.15 Pubchem ID :2783401
Synonyms :

Calculated chemistry of [ 319-24-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.08
TPSA : 52.32 ?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) : -5.37 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 2.77
Log Po/w (WLOGP) : 1.62
Log Po/w (MLOGP) : 1.75
Log Po/w (SILICOS-IT) : 1.4
Consensus Log Po/w : 1.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.87
Solubility : 0.227 mg/ml ; 0.00134 mol/l
Class : Soluble
Log S (Ali) : -3.52
Solubility : 0.0506 mg/ml ; 0.000299 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.39
Solubility : 0.692 mg/ml ; 0.00409 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.33

Safety of [ 319-24-4 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 319-24-4 ]

* 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 [ 319-24-4 ]

[ 319-24-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 23779-97-7 ]
  • [ 319-24-4 ]
  • [ 71638-41-0 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; triethylamine; In methanol; EXAMPLE 11 methyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluorobenzoate A solution of 16 g of 4-chloro-8-trifluoromethylquinoline, 11.62 g of methyl 2-amino-5-fluoro-benzoate and 70 ml of 2 N hydrochloric acid solution was heated to reflux and was allowed to stand overnight at room temperature. The mixture was iced and filtered and the product was empasted with a little water and was vacuum filtered. The recovered crystals were dissolved in methanol and triethylamine was added to the resulting solution until the pH was alkaline. The mixture was iced and filtered and the product was dried to obtain 11.2 g of methyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluoro-benzoate melting at 166 C.
  • 2
  • [ 319-24-4 ]
  • [ 147751-16-4 ]
  • tert-butyl ((2-(2-amino-5-fluorophenyl)-2-oxoethyl)sulfonyl)carbamate [ No CAS ]
  • 3
  • [ 117-21-5 ]
  • [ 319-24-4 ]
  • methyl 2-(4-chloro-1,3-dioxoisoindolin-2-yl)-5-fluorobenzoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
28% With acetic acid; at 110℃; for 4h; General procedure: The starting materials 1 and 2 were commercially available (Energy Chemical, Shanghai, China).Compound 2 (3.72 mmol) was added to a stirred solution of compound 1 (3.38 mmol) in glacial aceticacid (10 mL). The reaction mixture was then stirred at 110 C for 4 h. After completion of the reaction,the solvent was evaporated, and the residue was purified on a silica gel column chromatography andeluted with ethyl acetate/petroleum ether (bp 60-90 C) (1:3, v/v) to give compounds 3.
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