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[ CAS No. 654-76-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 654-76-2
Chemical Structure| 654-76-2
Structure of 654-76-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 654-76-2 ]

CAS No. :654-76-2 MDL No. :MFCD00007328
Formula : C8H6F3NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :KGFADEJSZXEVMC-UHFFFAOYSA-N
M.W : 221.13 Pubchem ID :69562
Synonyms :

Calculated chemistry of [ 654-76-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 6.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.76
TPSA : 55.05 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.66
Log Po/w (XLOGP3) : 2.61
Log Po/w (WLOGP) : 3.77
Log Po/w (MLOGP) : 1.68
Log Po/w (SILICOS-IT) : 0.75
Consensus Log Po/w : 2.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.95
Solubility : 0.246 mg/ml ; 0.00111 mol/l
Class : Soluble
Log S (Ali) : -3.42
Solubility : 0.0849 mg/ml ; 0.000384 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.8
Solubility : 0.35 mg/ml ; 0.00158 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.83

Safety of [ 654-76-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:1759
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 654-76-2 ]

* 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.

  • Upstream synthesis route of [ 654-76-2 ]

[ 654-76-2 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 654-76-2 ]
  • [ 393-15-7 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogen In methanol; water at 20℃; for 3.5 h; To a solution of 2-methoxy-5-nitrobenzotrifluoride (5.08 g, 23.0 mmol) in methanol (200 ml) was added 10percent Pd-C (containing 50percent water, 250 mg), and the resulting mixture was stirred for 3.5 hours under a hydrogen atmosphere at room temperature and atmospheric pressure while maintaining the temperature. The mixture was filtered by the use of Celite and the filtrate was concentrated to dryness under reduced pressure to obtain 4-methoxy-3-(trifluoromethyl)aniline (4.67 g, 100percent). MS : m/z = 192 (M + 1)
99% for 4 h; 1-Methoxy-4-nitro-2-trifluoromethyl-benzene (10 g, 45 mmol) was hydrogenated in a Paar apparatus with shaking at 50 psi for 4 hours, with 1 g 10 wt percent Pd/C.
The reaction mixture was filtered through celite, and the filtrate was evaporated in vacuo to give 8.6 g 4-Methoxy-3-trifluoromethyl-phenylamine, 99percent, as a solid.
99% for 4 h; 1-Methoxy-4-nitro-2-trifluoromethyl-benzene (10 g, 45 mmol) was hydrogenated in a Paar apparatus with shaking at 50 psi for 4 hours, with 1 g 10 wt percent Pd/C.
The reaction mixture was filtered through celite, and the filtrate was evaporated in vacuo to give 8.6 g 4-Methoxy-3-trifluoromethyl-phenylamine, 99percent, as a solid.
Reference: [1] Patent: EP1403255, 2004, A1, . Location in patent: Page 121
[2] Patent: US2005/209260, 2005, A1, . Location in patent: Page/Page column 143-144
[3] Patent: US2007/49609, 2007, A1, . Location in patent: Page/Page column 122
[4] Synthesis, 2006, # 19, p. 3316 - 3340
[5] Journal of Organic Chemistry, 1961, vol. 26, p. 2707 - 2710
[6] Patent: WO2003/99771, 2003, A2, . Location in patent: Page 138
[7] Patent: US6335350, 2002, B1, . Location in patent: Example 1
[8] Patent: EP1137645, 2004, B1, . Location in patent: Page 15
[9] Patent: WO2005/80340, 2005, A1, . Location in patent: Page/Page column 51
[10] Patent: FR745293, 1932, ,
  • 2
  • [ 654-76-2 ]
  • [ 7439-89-6 ]
  • [ 393-15-7 ]
Reference: [1] Patent: US6166028, 2000, A,
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