| Weight | 118.139 g/mol |
|---|---|
| Formula | C7H6N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-AZAINDOLE (272-49-1)
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- NOVEL OXO-BRIDGED BLUE LUMINESCENT ORGANOALUMINUM COMPLEXES : AL4(CH3)6(MU3-O)2(DPA)2 AND AL3(7-AZAIN)4(OCH(CF3)2)2(CH3)(MU 3-O) (DPA = DEPROTONATED DI-2-PYRIDYLAMINE, 7-AZAIN = DEPROTONATED 7-AZAINDOLE) (Organometallics, 1997)
- 7-azaindole and its clusters with Ar, CH sub 4 , H sub 2 O, NH sub 3 , and alcohols: Molecular geometry, cluster geometry, and nature of the first excited singlet electronic state (The Journal of Physical Chemistry, 1990)
- Blue Luminescent Organoaluminum Compounds: Al2(CH3)4(7-azain)2, Al2(CH3)2(7-azain)4, Al2(CH3)(OCH(CF3)2)3(7-azain)2, Al2(-OCH(CF3)2)(CH3)(7-azain)2((OCH(CF3)2)2, Al3(3-O)(CH3)(7-azain)4(OCH(CF3)2)2, and Al4(3-O)2(7-azain)6(OCH(CF3)2)2 (7-azain = Deprotonated 7-Azaindole) (Organometallics, 1998)
- Discovery of 1-[4-(3-Chlorophenylamino)-1-methyl-1H-pyrrolo[3,2-c]pyridin-7-yl]-1-morpholin-4-ylmethanone (GSK554418A), a Brain Penetrant 5-Azaindole CB2 Agonist for the Treatment of Chronic Pain (Journal of Medicinal Chemistry, 2009)
- Potent 4-amino-5-azaindole factor VIIa inhibitors (Bioorganic & Medicinal Chemistry Letters, 2006)
- Novel blue luminescent/electroluminescent 7-azaindole derivatives: 1,3-Di(N-7-azaindolyl)benzene, 1-bromo-3,5-Di(N-7-azaindolyl)benzene, 1,3,5-Tri(N-7-azaindolyl)benzene, and 4,4'-Di(N-7-azaindolyl)biphenyl (Chemistry of Materials, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CN2)N=C1
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InChIKeyXWIYUCRMWCHYJR-UHFFFAOYSA-N
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