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[ CAS No. 505084-59-3 ] {[proInfo.proName]}

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Chemical Structure| 505084-59-3
Chemical Structure| 505084-59-3
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Product Details of [ 505084-59-3 ]

CAS No. :505084-59-3 MDL No. :MFCD08741353
Formula : C7H3ClF3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :RMSKYTKOFDQVEL-UHFFFAOYSA-N
M.W : 225.55 Pubchem ID :12140227
Synonyms :

Calculated chemistry of [ 505084-59-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 6.0
Num. H-bond donors : 1.0
Molar Refractivity : 41.21
TPSA : 50.19 ?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) : -6.1 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.08
Log Po/w (XLOGP3) : 2.22
Log Po/w (WLOGP) : 3.6
Log Po/w (MLOGP) : 0.56
Log Po/w (SILICOS-IT) : 2.45
Consensus Log Po/w : 1.98

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.82
Solubility : 0.34 mg/ml ; 0.00151 mol/l
Class : Soluble
Log S (Ali) : -2.91
Solubility : 0.278 mg/ml ; 0.00123 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.91
Solubility : 0.278 mg/ml ; 0.00123 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.94

Safety of [ 505084-59-3 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 505084-59-3 ]

* 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 [ 505084-59-3 ]

[ 505084-59-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 35216-39-8 ]
  • [ 94790-37-1 ]
  • [ 505084-59-3 ]
  • 2-(benzotriazol-1-yloxy)-N-(3-methylsulfonylphenyl)-5-(trifluoromethyl)pyridine-3-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
61.9% With N-ethyl-N,N-diisopropylamine; In chloroform; at 20℃; for 40h; A mixture of 2-chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid (508 mg, 2.25 mmol), 3-methylsulfonylaniline (424 mg, 2.48 mmol), HBTU (854 mg, 2.25 mmol) and DIPEA (981 pL, 5.63 mmol) in chloroform (10 mL) was stirred at room temperature for 40 h. The solvent was removed under a stream of N2, and the residue treated with water/MeOH (5: 1). This mixture was briefly sonicated then stirred at room temperature for 24 h. The resulting precipitate was collected by filtration, washed with water and dried under vacuum to give 2-(benzotriazol-l-yloxy)-N-(3- methylsulfonylphenyl)-5-(trifluoromethyl)pyridine-3-carboxamide (665 mg, 1.39 mmol, 61.9% yield) as a beige solid. MS, ES+ m/z 448.0 [M+H]+.1H-NMR (400 MHz, DMSO-r e) d 11.37 (s, 1 H), 8.88 (d, J=2.27 Hz, 1 H), 8.72 (d, J= 1.01 Hz, 1 H), 8.43 (s, 1 H), 8.20 (d, J=8.59 Hz, 1 H), 8.03 - 8.07 (m, 1 H), 7.83 (d, J=8.59 Hz, 1 H), 7.67 - 7.77 (m, 3 H), 7.54 - 7.58 (m, 1 H), 3.25 (s, 3 H).
  • 2
  • [ 35216-39-8 ]
  • [ 505084-59-3 ]
  • 2-(2,4-dichlorophenoxy)-N-(3-methylsulfonylphenyl)-5-(trifluoromethyl)pyridine-3-carboxamide [ No CAS ]
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