| Weight | 181.238 g/mol |
|---|---|
| Formula | C13H11N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
9-Methylcarbazole (1484-12-4)
N-methylcarbazole
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- Design, Synthesis, and StructureActivity Correlations of Novel Dibenzo(b,d)furan, Dibenzo(b,d)thiophene, and N-Methylcarbazole Clubbed 1,2,3-Triazoles as Potent Inhibitors of Mycobacterium tuberculosis (Journal of Medicinal Chemistry, 2012)
- Reaction patterns and kinetics of the photoconversion of N- methyldiphenylamine to N-methylcarbazole (Journal of the American Chemical Society, 1973)
- The Formation of an N-Hydroxymethyl Intermediate in the N-Demethylation of N-Methylcarbazole in vivo and in vitro (Xenobiotica, 1976)
- Electrochemical Synthesis of N-Methylpyrrole and N-Methylcarbazole Copolymer on Carbon Fiber Microelectrodes, and Their Characterization (Turkish Journal of Chemistry, 2006)
- 18O incorporation from H218O2 in the oxidation of N-methylcarbazole and sulfides catalyzed by microperoxidase-11 (Tetrahedron Letters, 1992)
- Photoconversion of N-methyldiphenylamine to N-methylcarbazole. Calculated and observed quantum yields as a function of oxygen concentration (Journal of the American Chemical Society, 1974)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N-methylcarbazole
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SMILESCN1C2=CC=CC=C2C3=CC=CC=C31
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InChIKeySDFLTYHTFPTIGX-UHFFFAOYSA-N
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