Weight | 199.04 g/mol |
---|---|
Formula | C8H4Cl2N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
2,3-DICHLOROQUINOXALINE (2213-63-0)
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- New Techniques in Triplet State Phosphorescence Spectroscopy: Application to the Emission of 2,3Dichloroquinoxaline (Journal of Chemical Physics, 1971)
- Radiosensitization by 2-benzoyl-3-phenyl-6,7-dichloroquinoxaline 1,4-dioxide under oxia and hypoxia in human colon cancer cells (Radiation Oncology, 2007)
- Abolition of the NMDA-mediated responses by a specific glycine antagonist, 6,7-dichloroquinoxaline-2,3-dione (DCQX) (Biochemical and Biophysical Research Communications, 1989)
- 6,7Dichloroquinoxaline2,3Dione is a Competitive Antagonist Specific to StrychnineInsensitive [3H]Glycine Binding Sites on the NMethylDAspartate Receptor Complex (Journal of Neurochemistry, 1990)
- AlCl3 induced (hetero)arylation of 2,3-dichloroquinoxaline: A one-pot synthesis of mono/disubstituted quinoxalines as potential antitubercular agents (Bioorganic & Medicinal Chemistry, 2012)
- Observation of the set of the three sublevel phosphorescence spectra. III. External heavy atom effect on the phosphorescence spectra of quinoxaline and 2,3dichloroquinoxaline (Journal of Chemical Physics, 1981)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)N=C(C(=N2)Cl)Cl
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InChIKeySPSSDDOTEZKOOV-UHFFFAOYSA-N
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