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[ CAS No. 391-12-8 ] {[proInfo.proName]}

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Chemical Structure| 391-12-8
Chemical Structure| 391-12-8
Structure of 391-12-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 391-12-8 ]

CAS No. :391-12-8 MDL No. :MFCD01248408
Formula : C9H4F3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :MXLDJTXXAYVWDF-UHFFFAOYSA-N
M.W : 215.13 Pubchem ID :604575
Synonyms :

Calculated chemistry of [ 391-12-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.11
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.16
TPSA : 46.17 ?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) : -6.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.02
Log Po/w (XLOGP3) : 1.6
Log Po/w (WLOGP) : 2.42
Log Po/w (MLOGP) : 1.2
Log Po/w (SILICOS-IT) : 2.5
Consensus Log Po/w : 1.75

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.41
Solubility : 0.833 mg/ml ; 0.00387 mol/l
Class : Soluble
Log S (Ali) : -2.18
Solubility : 1.42 mg/ml ; 0.00659 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.67
Solubility : 0.0459 mg/ml ; 0.000213 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.86

Safety of [ 391-12-8 ]

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 [ 391-12-8 ]

* 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 [ 391-12-8 ]

[ 391-12-8 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 391-12-8 ]
  • [ 313-12-2 ]
YieldReaction ConditionsOperation in experiment
With dihydrogen peroxide; In sodium hydroxide; water; A. 3-Trifluoromethyl-2-aminobenzoic acid 7-Trifluoromethylisatin (10 g, 46 mmol) was dissolved in 5percent sodium hydroxide solution (83 ml). To this was added dropwise over 30 minutes a solution of 50percent hydrogen peroxide (7.4 ml) in water (4.6 ml); the temperature rose to 50°. The solution was stirred an additional 30 minutes, acidified (conc. HCl) to pH 1-2, and the tan product was filtered.
  • 3
  • [ 67-56-1 ]
  • [ 391-12-8 ]
  • [ 313-12-2 ]
  • [ 64321-95-5 ]
  • 4
  • [ 391-12-8 ]
  • [ 445-27-2 ]
  • [ 148887-60-9 ]
  • 5
  • [ 391-12-8 ]
  • [ 91-56-5 ]
  • [ 1150-98-7 ]
  • 6
  • [ 391-12-8 ]
  • [ 403-42-9 ]
  • [ 18060-39-4 ]
  • 7
  • [ 391-12-8 ]
  • [ 98-86-2 ]
  • [ 18193-08-3 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; In ethanol; at 0 - 80℃; for 24h; General procedure: Isatin (0.5 g, 3.34 mmol) was added into a stirred solution ofKOH (0.56 g, 10.02 mmol) in ethanol 10 ml at 80 C. The reactionmixture was stirred at 0 C for 24 h. The mixture was added to50 g ice water. The pH was adjusted by the solution of 2 N HCl to4?5. The mixture was cooled overnight and filtered. The residuewas recrystallized by the mixture of petroleum/ethyl acetate(5:1). Compound 4 (0.8 g) was obtained and the yield was 96.87percent.
  • 8
  • [ 391-12-8 ]
  • [ 100-06-1 ]
  • [ 18060-37-2 ]
  • 9
  • [ 391-12-8 ]
  • [ 2642-63-9 ]
  • [ 148887-62-1 ]
  • 11
  • [ 391-12-8 ]
  • [ 72985-53-6 ]
  • N-(2-Hydroxy-6-trifluoromethyl-phenyl)-oxalamic acid [ No CAS ]
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