6-Fluoro-2-methylquinoline, 98+%, Thermo Scientific Chemicals
6-Fluoro-2-methylquinoline, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

6-Fluoro-2-methylquinoline, 98+%, Thermo Scientific Chemicals

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100 g
5 g
25 g
Catalog number A11469.22
also known as A11469-22
Price (USD)/ Each
1,073.00
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Quantity:
100 g
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Price (USD)/ Each
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6-Fluoro-2-methylquinoline, 98+%, Thermo Scientific Chemicals
Catalog numberA11469.22
Price (USD)/ Each
1,073.00
-
Add to cart
Chemical Identifiers
CAS1128-61-6
IUPAC Name6-fluoro-2-methylquinoline
Molecular FormulaC10H8FN
InChI KeyGPIARMSVZOEZCV-UHFFFAOYSA-N
SMILESCC1=CC=C2C=C(F)C=CC2=N1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale cream to pale brown to gray
FormCrystals or powder or crystalline powder
Assay (GC)≥98.0%
Identification (FTIR)Conforms
Melting Point (clear melt)49.0-55.0?C
Metal-free transfer hydrogenation of 6-fluoro-2-methylquinoline by employing several chiral Bronsted acid catalysts was carried out in combination with dihydropyridines as the hydride source in asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation. Hydrogenation product of 6-fluoro-2-methylquinoline is the key intermediate of the antibacterial agent.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Metal-free transfer hydrogenation of 6-fluoro-2-methylquinoline by employing several chiral Brønsted acid catalysts was carried out in combination with dihydropyridines as the hydride source in asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation. Hydrogenation product of 6-fluoro-2-methylquinoline is the key intermediate of the antibacterial agent.

Solubility
Soluble in Chloroform.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Magnus Rueping,; Mirjam Stoeckel,; Erli Sugiono,; Thomas Theissmann. Asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation. Tetrahedron. 2010 , 6633,6565-6568.
  2. Nadia M. Ahmad,; Jie Jack Li. Palladium in Quinoline Synthesis. Advances in Heterocyclic Chemistry. 2003, 841-30.