Basic information Safety Supplier Related

6-QUINOXALINECARBOXYLIC ACID

Basic information Safety Supplier Related

6-QUINOXALINECARBOXYLIC ACID Basic information

Product Name:
6-QUINOXALINECARBOXYLIC ACID
Synonyms:
  • 6-QUINOXALINECARBOXYLIC ACID
  • IFLAB-BB F1716-0520
  • RARECHEM AM LA 0027
  • QUINOXALINE-6-CARBOXYLIC ACID
  • TIMTEC-BB SBB000185
  • CHINOXALIN-6-CARBONSAEURE
  • 6-Quinoxalinecarboxylic acid, 95+%
  • AKOS BBS-00001971
CAS:
6925-00-4
MF:
C9H6N2O2
MW:
174.16
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Quinoxalines
  • Aromatics
  • Heterocycles
  • Intermediates
  • Carboxylic Acids
  • Quinolines, Isoquinolines & Quinoxalines
  • Carboxylic Acids
  • Quinolines, Isoquinolines & Quinoxalines
Mol File:
6925-00-4.mol
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6-QUINOXALINECARBOXYLIC ACID Chemical Properties

Melting point:
224-229 °C (dec.)
Boiling point:
355.1±27.0 °C(Predicted)
Density 
1.421±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly, Sonicated)
form 
Solid
pka
3.22±0.30(Predicted)
color 
Light Brown to Dark Brown
InChI
InChI=1S/C9H6N2O2/c12-9(13)6-1-2-7-8(5-6)11-4-3-10-7/h1-5H,(H,12,13)
InChIKey
JGQDBVXRYDEWGM-UHFFFAOYSA-N
SMILES
N1C2C(=CC(C(O)=O)=CC=2)N=CC=1
CAS DataBase Reference
6925-00-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900
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6-QUINOXALINECARBOXYLIC ACID Usage And Synthesis

Chemical Properties

Tan Solid

Uses

6-Quinoxalinecarboxylic Acid is an intermediate used in the production of antiprotozoal agents.

Synthesis

131543-46-9

619-05-6

6925-00-4

Stage 1: The compound (CAS:131543-46-9) was reacted with 3,4-diaminobenzoic acid in a mixed solvent of ethanol and acetic acid with glyoxal at 75 °C. After completion of the reaction, the resulting suspension was cooled to 5 °C and filtered. The collected wet cake of 6-quinoxaline carboxylic acid was washed with cold ethanol and subsequently dried under vacuum at 50 °C.

References

[1] Patent: US2007/179144, 2007, A1. Location in patent: Page/Page column 5; 6
[2] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 4, p. 815 - 820
[3] Patent: US2009/286797, 2009, A1. Location in patent: Page/Page column 6
[4] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 14, p. 3771 - 3774
[5] European Journal of Medicinal Chemistry, 2012, vol. 48, p. 255 - 264

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