| Weight | 162.148 g/mol |
|---|---|
| Formula | C8H6N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
7-Nitroindole (6960-42-5)
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- The 7Nitroindole Nucleoside as a Photochemical Precursor of 2Deoxyribonolactone: Access to DNA Fragments Containing This Oxidative Abasic Lesion (Chemistry: A European Journal, 2000)
- Protein kinase C modulators. Indolactams. 2.1 Alkylation of 4-nitroindole by Grignard reagents. Synthesis of (-)-7-octylindolactam V (Tetrahedron Letters, 1994)
- Hybridization properties and enzymatic replication of oligonucleotides containing the photocleavable 7-nitroindole base analog (Nucleic Acids Research, 2005)
- Notes - Synthesis of 7-Nitroindole (Journal of Organic Chemistry, 1957)
- Mycophenolic Acid, Mycophenolate Mofetil, Mizoribine, Ribavirin, and 7-Nitroindole Inhibit Propagation of Babesia Parasites by Targeting Inosine 5-Monophosphate Dehydrogenase (Journal of Parasitology, 2014)
- Synthesis of 4, 5, 6 and 7Nitroindole2methanols and 4, 5, 6 and 7Nitroindole2carbaldehydes. (ChemInform, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C(=C1)[N+](=O)[O-])NC=C2
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InChIKeyLZJGQIVWUKFTRD-UHFFFAOYSA-N
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