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[ CAS No. 54396-44-0 ] {[proInfo.proName]}

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Chemical Structure| 54396-44-0
Chemical Structure| 54396-44-0
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Quality Control of [ 54396-44-0 ]

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Product Details of [ 54396-44-0 ]

CAS No. :54396-44-0 MDL No. :MFCD00153216
Formula : C8H8F3N Boiling Point : -
Linear Structure Formula :- InChI Key :TWLDBACVSHADLI-UHFFFAOYSA-N
M.W : 175.15 Pubchem ID :2735932
Synonyms :

Calculated chemistry of [ 54396-44-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.81
TPSA : 26.02 ?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) : -5.6 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.74
Log Po/w (XLOGP3) : 2.49
Log Po/w (WLOGP) : 3.76
Log Po/w (MLOGP) : 2.88
Log Po/w (SILICOS-IT) : 2.57
Consensus Log Po/w : 2.69

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.8
Solubility : 0.278 mg/ml ; 0.00159 mol/l
Class : Soluble
Log S (Ali) : -2.68
Solubility : 0.365 mg/ml ; 0.00208 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.31
Solubility : 0.0862 mg/ml ; 0.000492 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.13

Safety of [ 54396-44-0 ]

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 [ 54396-44-0 ]

* 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 [ 54396-44-0 ]

[ 54396-44-0 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 54396-44-0 ]
  • [ 16497-87-3 ]
  • N-3-(trifluoromethyl)phenylanthranilic acid [ No CAS ]
  • 2
  • [ 54396-44-0 ]
  • [ 1452-94-4 ]
  • [ 54396-42-8 ]
  • 3
  • [ 150783-50-9 ]
  • [ 54396-44-0 ]
YieldReaction ConditionsOperation in experiment
98.5% With hydrogenchloride; In ethanol; Preparation of 2-Methyl-3-Trifluoromethyl-Aniline A solution of 2,2,2'-trimethyl-3'-trifluoromethyl-propionanilide (10 g.) in 75 ml. ethanol and 75 ml. concentrated HCl was refluxed for 24 hours. The reaction mixture was then concentrated in vacuo and diluted with water. It was then basified with 10percent NaOH solution and extracted with ether. The ether extract was washed with water and brine and dried with MgSO4. Removal of ether gave a pale brown liquid (6.65 g., 98.5percent) which was purified by distillation under reduced pressure (b.p. 108°-110° C., 30 mm.) to give 5.73 g. of 2-methyl-3-trifluoromethyl-aniline which solidified on standing. The physical and spectroscopic properties of the product were found to be identical to those of an authentic sample of 2-methyl-3-trifluoromethyl-aniline prepared by the known method below. STR2
YieldReaction ConditionsOperation in experiment
96% The CH2 Cl2 extracts are dried over K2 CO3 and evaporated to give 2-methyl-3-trifluoromethyl-aniline (MTA) (6.5 g, 96percent yield), an oil which solidifies on standing. STR13 iv.) A mixture of 2-methyl-3-trifluoromethylaniline (368 g, 2.1 moles) and 2-chloronicotinic acid (158.0 9, 1.0 mole) in 400 ml of water is heated at 100° C. for 24 hours together with p-toluenesulfonic acid (15.0 g) monohydrate as the acid catalyst. Potassium hydroxide (ca. 145 g) in water (255 ml) is added and the pH is maintained above 11. After diluting the reaction mixture to 1.2 liters with water, the mixture is cooled to 50° C., adjusted to pH 11, treated with 7 g of a decolorizing charcoal and 15 g of a filter aid, and clarified by filtration. The filtrate is diluted with 750 ml of water and the pH is adjusted to 5.0 with concentrated sulfuric acid.
96% iii.) 2-methyl-3-trifluoromethylpivalanilide (10.0 g)is hydrolyzed by refluxing in concentrated HBr (40 ml, 48percent) for 3 hours. The mixture is cooled to 20° C. and poured onto ice-water (40.0 g). The pH is adjusted to 9 with concentrated NaOH and the mixture is extracted with two. 30 ml portions of CH2 Cl2. The CH2 Cl2 extracts are dried over K2 CO3 and evaporated to give 2-methyl-3-trifluoromethyl-aniline (MTA) (6.5 g, 96percent yield), an oil which solidifies on standing. STR13
Following the procedure of Example 1, the following substituted aniline compounds:...3-fluoro-2-methylaniline3-iodo-2-methylaniline3-trifluoromethyl-2-methylaniline
  • 5
  • [ 56-23-5 ]
  • [ 95-53-4 ]
  • [ 25449-96-1 ]
  • [ 54396-44-0 ]
  • 6
  • [ 1019327-29-7 ]
  • [ 54396-44-0 ]
  • [ 913067-77-3 ]
  • 7
  • 3-(2-amino-quinazolin-6-yl)-4-methyl-benzoyl chloride [ No CAS ]
  • [ 54396-44-0 ]
  • 3-(2-amino-6-quinazolinyl)-4-methyl-N-(2-methyl-3-(trifluoromethyl)phenyl)benzamide [ No CAS ]
  • 8
  • [ 54396-44-0 ]
  • [ 108-24-7 ]
  • [ 546434-38-2 ]
  • 9
  • [ 54396-44-0 ]
  • [ 98-59-9 ]
  • [ 947407-68-3 ]
  • 10
  • [ 54396-44-0 ]
  • C26H24N3SO4F3 [ No CAS ]
  • 11
  • [ 54396-44-0 ]
  • [ 947407-70-7 ]
  • 12
  • [ 54396-44-0 ]
  • [ 947407-75-2 ]
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