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[ CAS No. 72505-21-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 72505-21-6
Chemical Structure| 72505-21-6
Structure of 72505-21-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 72505-21-6 ]

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Product Details of [ 72505-21-6 ]

CAS No. :72505-21-6 MDL No. :MFCD00051806
Formula : C8H6F3NS Boiling Point : No data available
Linear Structure Formula :- InChI Key :IPRFNMJROWWFBH-UHFFFAOYSA-N
M.W : 205.20 Pubchem ID :2734823
Synonyms :

Calculated chemistry of [ 72505-21-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.91
TPSA : 58.11 ?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) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.74
Log Po/w (XLOGP3) : 2.31
Log Po/w (WLOGP) : 3.49
Log Po/w (MLOGP) : 2.79
Log Po/w (SILICOS-IT) : 3.46
Consensus Log Po/w : 2.76

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.78
Solubility : 0.343 mg/ml ; 0.00167 mol/l
Class : Soluble
Log S (Ali) : -3.17
Solubility : 0.139 mg/ml ; 0.000678 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.08
Solubility : 0.17 mg/ml ; 0.000826 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.43

Safety of [ 72505-21-6 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P280-P305+P351+P338-P311 UN#:2811
Hazard Statements:H301+H311+H331-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 72505-21-6 ]

* 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 [ 72505-21-6 ]

[ 72505-21-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 70-23-5 ]
  • [ 72505-21-6 ]
  • [ 175204-88-3 ]
YieldReaction ConditionsOperation in experiment
63% In acetone; for 3h;Heating / reflux; To a stirred solution of 4-trifluoromethylthiobenzamide (205 g, 10 mmol) in acetone (10 mL) was added ethyl bromopyruvate (1.95 g, 10 mmol) in acetone (10 mL) dropwise. The mixture was stirred under reflux for 3 h. After cooling to room temperature, the solution was concentrated and purified by column chromatography to give 1.9 g (63%) of cpd Q1 as a white solid: 1H NMR (300 MHz, CDCl3) δ 8.23 (s, 1H), 8.14 (d, J=8.4 Hz, 2H), 7.72 (d, J=8.4 Hz, 2H), 4.46 (q, J=7.1 Hz, 2H) 1.44(t, J=7.1 Hz, 3H); MS (ES) m/z: 302 (M+H+).
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