6-Methoxyquinoline

6-Methoxyquinoline
  • CAS No.:5263-87-6
Other grades of this product :
6-Methoxyquinoline Basic information
Product Name:6-Methoxyquinoline
Synonyms:6-METHOXYQUINOLINE;Methoxyquinoline,95%;6-Methoxyquinoline, 98+%;6-quinanisole;6-Methoxyquinoline, 98% 25GR;NSC 1954;6-Methoxyquinoline6-;6-Methoxy-1-azanaphthalene
CAS:5263-87-6
MF:C10H9NO
MW:159.18
EINECS:226-077-2
Product Categories:Chemical Amines;Alkoxyquinolines;Quinolines;Amines;Aromatics;Building Blocks;Quinoline&Isoquinoline;Heterocyclic Building Blocks;5263-87-6
Mol File:5263-87-6.mol
6-Methoxyquinoline Chemical Properties
Melting point 18-20 °C (lit.)
Boiling point 140-146 °C/15 mmHg (lit.)
density 1.15 g/mL at 20 °C (lit.)
refractive index n20/D 1.625(lit.)
FEMA 4640 | 6-METHOXYQUINOLINE
Fp >230 °F
storage temp. Store below +30°C.
solubility soluble in Alcohol
pka5.03(at 20℃)
form Granular Powder
color White to cream
Water Solubility insoluble
Sensitive Light Sensitive
JECFA Number2157
BRN 115244
CAS DataBase Reference5263-87-6(CAS DataBase Reference)
NIST Chemistry ReferenceQuinoline, 6-methoxy-(5263-87-6)
EPA Substance Registry SystemQuinoline, 6-methoxy- (5263-87-6)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 23-24/25-36-26
WGK Germany 3
8
TSCA Yes
HS Code 29334990
MSDS Information
ProviderLanguage
6-Methoxyquinoline English
ACROS English
SigmaAldrich English
ALFA English
6-Methoxyquinoline Usage And Synthesis
Chemical Propertiescolorless to light yellow liquid
Uses6-Methoxyquinoline is a useful sythetic intermediate
Uses6-Methoxyquinoline is used as a precursor in the synthesis of:
  • Fluorescent zinc and chlorine sensors.
  • 5-Amino-2-aroylquinolines as potent tubulin polymerization inhibitors.
  • 3-Fluoro-6-methoxyquinoline derivatives as inhibitors of bacterial DNA gyrase and topoisomerase.
  • Cobalt-based ternary metal-organic complex as single?ion magnets.
DefinitionChEBI: An aromatic ether that is quinoline substituted at position 6 by a methoxy group.
Synthesis Reference(s)Journal of the American Chemical Society, 68, p. 1584, 1946 DOI: 10.1021/ja01212a062

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