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2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLINE

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2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLINE Basic information

Product Name:
2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLINE
Synonyms:
  • 2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLINE
  • 4-BROMO-2,8-BIS(TRIFLUOROMETHYL)QUINOLINE
  • 2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLIN
  • 4-Bromo-2,8-bis(trifluoromethyl)quinoline, >=98%
  • 1-METHYL-3-(AMINOMETHYL)PIPERIDINE
  • 2,8-BIS(TRIFL
  • Quinoline, 4-bromo-2,8-bis(trifluoromethyl)-
  • )-4-BROMOQUINOL
CAS:
35853-45-3
MF:
C11H4BrF6N
MW:
344.05
EINECS:
609-183-7
Product Categories:
  • Quinoline series
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Quinolines
  • QuinolinesHeterocyclic Building Blocks
Mol File:
35853-45-3.mol
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2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLINE Chemical Properties

Melting point:
62-64 °C(lit.)
Boiling point:
281.6±35.0 °C(Predicted)
Density 
1.720±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Crystalline Powder
pka
-3.67±0.50(Predicted)
color 
Off-white to yellow
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
2933499090

MSDS

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2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLINE Usage And Synthesis

Synthesis

35853-41-9

35853-45-3

Under argon protection, phosphorus bromide oxide (4 g, 14.2 mmol) was heated to 90 °C until the solid was completely dissolved. To this hot solution was added 2,8-bis(trifluoromethyl)-4-hydroxyquinoline (4.08 g, 14.2 mmol) and the temperature of the oil bath was raised to 150 °C. After 6 hours of reaction, the mixture was cooled to room temperature. The reaction was quenched by the addition of ice water and the resulting precipitate was filtered and washed with cold water to afford the target product 4-bromo-2,8-bis(trifluoromethyl)quinoline (4.70 g, 96% yield) as a white solid. Thin layer chromatography (TLC) Rf value was 0.79 (unfolding agent: cyclohexane/ether=5:1). Melting point: 60°C. 1H NMR (300 MHz, CDCl3) δ 7.82 (t, J=7.9 Hz, 1H), 8.11 (s, 1H), 8.22 (d, J=7.3 Hz, 1H), 8.46 (d, J=8.6 Hz, 1H). 13C NMR (125 MHz, CDCl3) δ 120.9 (q, J= 276.0 Hz), 122.0 (q, J=2.0 Hz), 123.6 (q, J=273.8 Hz), 128.9, 129.4, 129.8 (q, J=30.8 Hz), 130.5 (q, J=5.3 Hz), 131.5, 138.5, 144.5, 148.6 (q, J=36.1 Hz). Infrared spectra (IR) νmax: 1577, 1422, 1302, 1136, 1098, 1010, 876, 824 cm-1. gas chromatography-mass spectrometry (GC-MS) m/z: 343. high-resolution mass spectrometry (HRMS) calculated value of C11H4BrF6Na(M+Na)+: 365.9329, measured value: 365.9346.

References

[1] Angewandte Chemie - International Edition, 2015, vol. 54, # 47, p. 14070 - 14074
[2] Angew. Chem., 2015, vol. 127, # 47, p. 14276 - 14280,5
[3] Journal of Organic Chemistry, 2016, vol. 81, # 20, p. 9567 - 9575
[4] Tetrahedron Asymmetry, 2011, vol. 22, # 2, p. 138 - 148
[5] Patent: WO2012/107532, 2012, A1. Location in patent: Page/Page column 20-21

2,8-BIS(TRIFLUOROMETHYL)-4-BROMOQUINOLINESupplier

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