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[ CAS No. 66684-57-9 ] {[proInfo.proName]}

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Chemical Structure| 66684-57-9
Chemical Structure| 66684-57-9
Structure of 66684-57-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 66684-57-9 ]

CAS No. :66684-57-9 MDL No. :MFCD00456804
Formula : C6H2F3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :MXOQPGDHOAMPJW-UHFFFAOYSA-N
M.W : 177.08 Pubchem ID :3017703
Synonyms :

Calculated chemistry of [ 66684-57-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 35.14
TPSA : 45.82 ?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) : -5.92 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.28
Log Po/w (XLOGP3) : 2.05
Log Po/w (WLOGP) : 3.27
Log Po/w (MLOGP) : 2.98
Log Po/w (SILICOS-IT) : 1.0
Consensus Log Po/w : 2.12

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.53
Solubility : 0.519 mg/ml ; 0.00293 mol/l
Class : Soluble
Log S (Ali) : -2.64
Solubility : 0.405 mg/ml ; 0.00229 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.61
Solubility : 0.431 mg/ml ; 0.00243 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.88

Safety of [ 66684-57-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 66684-57-9 ]

* 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 [ 66684-57-9 ]

[ 66684-57-9 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 617-86-7 ]
  • [ 5580-79-0 ]
  • [ 358-43-0 ]
  • [ 66684-57-9 ]
Reference: [1] Journal of the American Chemical Society, 2012, vol. 134, # 39, p. 16216 - 16227,12
  • 2
  • [ 367-23-7 ]
  • [ 66684-57-9 ]
Reference: [1] Journal of Organic Chemistry, 1995, vol. 60, # 22, p. 7348 - 7350
  • 3
  • [ 5580-79-0 ]
  • [ 66684-57-9 ]
  • [ 66684-58-0 ]
Reference: [1] Advanced Synthesis and Catalysis, 2012, vol. 354, # 8, p. 1529 - 1541
[2] Angewandte Chemie - International Edition, 2013, vol. 52, # 11, p. 3203 - 3207[3] Angew. Chem., 2013, vol. 125, # 11, p. 3285 - 3289,5
  • 4
  • [ 361-39-7 ]
  • [ 66684-57-9 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 5
  • [ 366-50-7 ]
  • [ 66684-57-9 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 6
  • [ 880-78-4 ]
  • [ 6257-03-0 ]
  • [ 5580-79-0 ]
  • [ 66684-57-9 ]
Reference: [1] Advanced Synthesis and Catalysis, 2012, vol. 354, # 8, p. 1529 - 1541
  • 7
  • [ 880-78-4 ]
  • [ 66684-57-9 ]
  • [ 66684-58-0 ]
Reference: [1] Advanced Synthesis and Catalysis, 2012, vol. 354, # 8, p. 1529 - 1541
[2] Advanced Synthesis and Catalysis, 2012, vol. 354, # 8, p. 1529 - 1541
[3] Angewandte Chemie - International Edition, 2013, vol. 52, # 11, p. 3203 - 3207[4] Angew. Chem., 2013, vol. 125, # 11, p. 3285 - 3289,5
[5] Angewandte Chemie - International Edition, 2013, vol. 52, # 11, p. 3203 - 3207[6] Angew. Chem., 2013, vol. 125, # 11, p. 3285 - 3289,5
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