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6-Bromo-2-methylquinoline

Basic information Safety Supplier Related

6-Bromo-2-methylquinoline Basic information

Product Name:
6-Bromo-2-methylquinoline
Synonyms:
  • 6-BROMOQUINAIDINE
  • 6-BROMO-2-METHYLQUINOLINE
  • 6-BROMOQUINALDINE
  • 6-Bromoquinaldine, 6-Bromo-2-methyl-1-azanaphthalene
  • 6-BroMo-2-Methylquinoline, 97+%
  • Quinoline, 6-bromo-2-methyl-
  • 6-Bromoquildine, 98%
  • 6-Bromo-2-methylquinoline >
CAS:
877-42-9
MF:
C10H8BrN
MW:
222.08
Product Categories:
  • Quinoline&Isoquinoline
  • Alkylquinolines
  • Haloquinolines
  • Quinolines
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • QuinolinesHeterocyclic Building Blocks
Mol File:
877-42-9.mol
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6-Bromo-2-methylquinoline Chemical Properties

Melting point:
101-105 °C (lit.)
Boiling point:
299.7±20.0 °C(Predicted)
Density 
1.488±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
pka
5.02±0.43(Predicted)
form 
solid
color 
Grey
InChIKey
SQRYQSKJZVQJAY-UHFFFAOYSA-N
CAS DataBase Reference
877-42-9(CAS DataBase Reference)
NIST Chemistry Reference
6-Bromoquinaldine(877-42-9)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-37/38-42-36/37/38-20/21/22
Safety Statements 
26-39-36/37/39-24/25-22
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29339900

MSDS

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6-Bromo-2-methylquinoline Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Synthesis

106-40-1

123-73-9

877-42-9

GENERAL METHOD: 4-Bromoaniline (1.50 mmol) and trans-2-butenal (1.00 mmol) were dissolved in 1.5 mL of ether (Et2O) in a reaction flask fitted with a magnetic stir bar, followed by the addition of silver(I)-exchanged montmorillonite K10 (0.50 g). After stirring for 5 min, the solvent was removed under vacuum to obtain a dry powder. The reaction mixture was heated at 120 °C for 3 hours. After the reaction mixture was cooled to room temperature, it was filtered through a short silica gel plug and the solid residue was washed well with dichloromethane (CH2Cl2). After removal of the solvent under vacuum, the crude product was purified by silica gel column chromatography, eluting using a solvent mixture of hexane/ethyl acetate (EtOAc) to give the final 6-bromo-2-methylquinoline (3a-3k). Note: For recycling/reuse studies, the crude product is separated by gravity filtration and the clay material is washed several times with dichloromethane (CH2Cl2), air-dried and weighed. The process is repeated for successive recycling/reuse reactions.

References

[1] Advanced Functional Materials, 2012, vol. 22, # 2, p. 345 - 352
[2] Heterocycles, 2016, vol. 92, # 12, p. 2213 - 2224
[3] Tetrahedron Letters, 2011, vol. 52, # 22, p. 2840 - 2843
[4] Chemical Communications, 2012, vol. 48, # 35, p. 4196 - 4198
[5] Dalton Transactions, 2012, vol. 41, # 20, p. 6189 - 6194

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