| Weight | 162.148 g/mol |
|---|---|
| Formula | C8H6N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-Nitroindole (4769-97-5)
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- Electrochemical behaviour of nitroindoles: oxidative electropolymerization and reduction of the nitro group of polymerized and non-polymerized 4-nitro and 5-nitroindole (Journal of Electroanalytical Chemistry, 1996)
- A novel method of indole ring system construction: One-pot synthesis of 4- and 6- nitroindole derivatives via base promoted reaction between 3-nitroaniline and ketones (Tetrahedron Letters, 1999)
- Simple syntheses of 1,3,4,5-tetrahydropyrrole[4,3,2-DE}-quinoline and 5-hydroxy-4-nitroindole (synthetic study for indole having a nitrogen containing functional group at the 4-position) (Heterocycles, 1991)
- Protein kinase C modulators. Indolactams. 2.1 Alkylation of 4-nitroindole by Grignard reagents. Synthesis of (-)-7-octylindolactam V (Tetrahedron Letters, 1994)
- Selectivities of Multicomponent [4 + 2]/[3 + 2] Cycloadditions of 3-Nitroindole with Substituted Alkenes: A DFT Analysis (Journal of Organic Chemistry, 2013)
- Thiourea-catalyzed dearomatizing [4+2] cycloadditions of 3-nitroindole (Catalysis Communications, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CN2)C(=C1)[N+](=O)[O-]
-
InChIKeyLAVZKLJDKGRZJG-UHFFFAOYSA-N
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