Quinoline-5-carboxylic acid, 97+%
Quinoline-5-carboxylic acid, 97+%
Quinoline-5-carboxylic acid, 97+%
Quinoline-5-carboxylic acid, 97+%
Thermo Scientific Chemicals

Quinoline-5-carboxylic acid, 97+%

CAS: 7250-53-5 | C10H7NO2 | 173.17 g/mol
Quantity:
250 mg
1 g
5 g
Catalog number L19643.06
also known as L19643-06
Price (JPY)
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Quantity:
5 g
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Chemical Identifiers
CAS7250-53-5
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream to pale brown to pale gray
FormPowder
Assay (Non-aqueous acid-base Titration)≥97.0 to ≤103.0%
Assay (HPLC)≥97.0%
Melting Point (clear melt)295.0-305.0?C
Quinoline-5-carboxylic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.

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
Quinoline-5-carboxylic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.

Solubility
Slightly soluble in water.

Notes
Keep the container tightly sealed. Store in a cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Robert Musiol.; Josef Jampilek.; Katarina Kralova.; Des R. Richardson.; Danuta Kalinowski.; Barbara Podeszwa.; Jacek Finster.; Halina Niedbala.; Anna Palka.; Jaroslaw Polanski. Investigating biological activity spectrum for novel quinoline analogues. Bioorganic & Medicinal Chemistry. 2007, 15 (3), 1280-1288.
  2. I. V. Ukrainets.; N. Yu. Golik.; A. L. Shemchuk.; O. I. Naboka.; Yu. V. Voronina.; A. V. Turov. 4-hydroxy-2-quinolones. 197*. The search for novel diuretics amongst halo-substituted 6-hydroxy-2-methyl-4-oxo-1,2-dihydro-4H-pyrrolo-[3,2,1-ij]quinoline-5-carboxylic acid anilides. Chemistry of Heterocyclic Compounds. 2011, 47 (7), 826-832.