6-Bromoquinoline

Suppliers

Names

[ CAS No. ]:
5332-25-2

[ Name ]:
6-Bromoquinoline

[Synonym ]:
Quinoline, 6-bromo-
MFCD00024023
6-Bromoquinoline
EINECS 206-363-3

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
278.0±0.0 °C at 760 mmHg

[ Melting Point ]:
19°C

[ Molecular Formula ]:
C9H6BrN

[ Molecular Weight ]:
208.06

[ Flash Point ]:
132.8±19.8 °C

[ Exact Mass ]:
206.968353

[ PSA ]:
12.89000

[ LogP ]:
2.83

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.674

[ Storage condition ]:
Refrigerator

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302-H315-H318-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39-S39

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933499090

Customs

[ HS Code ]: 2933499090

[ Summary ]:
2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Direct, catalytic, and regioselective synthesis of 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles from N-oxides.

Org. Lett. 16(3) , 864-7, (2014)

A one-step transformation of heterocyclic N-oxides to 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles is described. The success of this broad-scope methodology hinges on the combination of cop...


More Articles


Related Compounds

  • 6-bromoquinoline 1-oxide
  • 6-bromoquinoline-8-thiol
  • 8-amino-6-bromoquinoline
  • 4-Amino-6-bromoquinoline
  • 5-Amino-6-bromoquinoline
  • 2-Amino-6-bromoquinoline
  • 2-fluoro-N-(4-fluoro-2-methylphenyl)pyridine-4-carboxamide
  • N-(4-cyclopentyloxyphenyl)-2-fluoropyridine-4-carboxamide
  • 2-fluoro-N-[2-(furan-2-yl)ethyl]pyridine-4-carboxamide
  • methyl N-[(1-methyl-1H-indol-5-yl)carbonyl]glycinate
  • N-(1-cyano-1-cyclopropylethyl)-2-{cyclopropyl[1-(2-fluorophenyl)ethyl]amino}acetamide
  • N-(1-cyano-1-cyclopropylethyl)-2-{[2,2-dimethyl-1-(thiophen-2-yl)propyl]amino}acetamide
  • Methyl 2-[(4-chlorophenyl)methyl-[2-[(1-cyanocyclopentyl)amino]-2-oxoethyl]amino]acetate
  • Methyl 2-{[(2-chlorophenyl)methyl]({[(1-cyanocyclopentyl)carbamoyl]methyl})amino}acetate
  • (2-Ethoxyethyl)[1-(5-methylthiophen-2-yl)ethyl]amine
  • 3,5-dimethyl-1-{5-propyl-5H-[1,2,4]triazino[5,6-b]indol-3-yl}-1H-pyrazole
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