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[ CAS No. 27407-11-0 ] {[proInfo.proName]}

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Chemical Structure| 27407-11-0
Chemical Structure| 27407-11-0
Structure of 27407-11-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 27407-11-0 ]

CAS No. :27407-11-0 MDL No. :MFCD03425884
Formula : C6H4BrFO Boiling Point : -
Linear Structure Formula :- InChI Key :QWTULQLVGNZMLF-UHFFFAOYSA-N
M.W : 191.00 Pubchem ID :2783381
Synonyms :

Calculated chemistry of [ 27407-11-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 36.12
TPSA : 20.23 ?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) : -5.79 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 2.36
Log Po/w (WLOGP) : 2.71
Log Po/w (MLOGP) : 2.67
Log Po/w (SILICOS-IT) : 2.48
Consensus Log Po/w : 2.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.0
Solubility : 0.189 mg/ml ; 0.00099 mol/l
Class : Soluble
Log S (Ali) : -2.43
Solubility : 0.718 mg/ml ; 0.00376 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.96
Solubility : 0.211 mg/ml ; 0.00111 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.5

Safety of [ 27407-11-0 ]

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

Application In Synthesis of [ 27407-11-0 ]

* 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 [ 27407-11-0 ]

[ 27407-11-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 27407-11-0 ]
  • [ 19047-31-5 ]
  • [ 1549559-40-1 ]
YieldReaction ConditionsOperation in experiment
66% With potassium carbonate; In acetone; at 60℃; for 16h; A solution of <strong>[19047-31-5]2-chloro-N-cyclopropylacetamide</strong> (1.7 g, 13.1 mmol), 3-bromo- 4-fluorophenol (2.5 g, 13.1 mmol) and K2CO3 (2.7 g, 19.6 mmol) in 20 mL of acetone was heated at 60 C for 16 h. The mixture was filtered and concentrated to give a residue, which was purified by column chromatography (PE/EA, 3/1) to give the title compound (2.5 g, 66%) as a yellow solid, m/e 289 (M+H)+.
66% With potassium carbonate; In acetone; at 60℃; for 16h; Example 80 2-(3-Bromo-4-fluorophenoxy)-N-cyclopropylacetamide A solution of <strong>[19047-31-5]2-chloro-N-cyclopropylacetamide</strong> (1.7 g, 13.1 mmol), 3-bromo-4- fluorophenol (2.5 g, 13.1 mmol) and K2C03 (2.7 g, 19.6 mmol) in 20 mL of acetone was heated at 60 C for 16 h. The mixture was filtered and concentrated to give a residue, which was purified by column chromatography (PE/EA, 3/1) to give the title compound (2.5 g, 66%) as a yellow solid, m/e 289 (M+H)+.
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