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Sigma-Aldrich

2-Quinoxalinecarboxylic acid

97%

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About This Item

Fórmula empírica (notación de Hill):
C9H6N2O2
Número de CAS:
879-65-2
Peso molecular:
174.16
MDL number:
MFCD00012334
UNSPSC Code:
12352100
PubChem Substance ID:
24857655
NACRES:
NA.22

assay

97%

mp

208 °C (dec.) (lit.)

SMILES string

OC(=O)c1cnc2ccccc2n1

InChI

1S/C9H6N2O2/c12-9(13)8-5-10-6-3-1-2-4-7(6)11-8/h1-5H,(H,12,13)

InChI key

UPUZGXILYFKSGE-UHFFFAOYSA-N

General description

Linear and Freundlich adsorption isotherm coefficient of 2-quinoxalinecarboxylic acid has been evaluated.

Application

2-Quinoxalinecarboxylic acid has been used in the preparation of:
  • N-(2-quinoxaloyl)-α-amino acids
  • bisquinoxaloyl (bisquinoxalinecarbonyl) derivatives

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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N Prabavathi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 92, 325-335 (2012-03-27)
The FTIR and FT-Raman spectra of 2-quinoxaline carboxylic acid (2-QCA) has been recorded in the region 4000-450 and 4000-100 cm(-1), respectively. The conformational analysis, optimized geometry, frequency and intensity of the vibrational bands of 2-QCA were obtained by the density
M D Rose et al.
Food additives and contaminants, 12(2), 177-183 (1995-03-01)
A method for the determination of residues of quinoxaline-2-carboxylic acid (QCA), the major metabolite of carbadox, in pig kidney has been developed. Tissue samples were subjected to alkaline hydrolysis, liquid-liquid extractions, ion-exchange chromatography and further extraction to concentrate the analyte
Joshua A Hagen et al.
Sensors (Basel, Switzerland), 11(7), 6645-6655 (2011-12-14)
Zinc oxide field effect transistors (ZnO-FET), covalently functionalized with single stranded DNA aptamers, provide a highly selective platform for label-free small molecule sensing. The nanostructured surface morphology of ZnO provides high sensitivity and room temperature deposition allows for a wide
Alex P Praseuth et al.
Biotechnology progress, 24(1), 134-139 (2008-01-05)
Proficient production of the antitumor agent triostin A was developed using engineered Escherichia coli (E. coli). The bacterium played host to 15 genes that encode integral biosynthetic proteins which were identified and cloned from Streptomyces lasaliensis. In this study, triostin
Kento Koketsu et al.
Organic letters, 8(21), 4719-4722 (2006-10-06)
[reaction: see text] Little is known about how quinoxaline-2-carboxylic acid (QC) is synthesized in nature. On the basis of analysis of echinomycin biosynthetic gene clusters as well as feeding experiments with labeled precursors, we have proposed a biosynthetic pathway to
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