Weight | 181.238 g/mol |
---|---|
Formula | C13H11N |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 1 |
Aromatic Rings | 3 |
Rotatable Bonds | 0 |
2-METHYLCARBAZOLE (3652-91-3)
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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)
- The Reaction of Substituted Indoles with Methyl Vinyl Ketone. New Synthesis of 2-Methylcarbazole (Journal of the American Chemical Society, 1957)
- Thermodynamic and Thermophysical Properties of Organic Nitrogen Compounds. Part II. 1 and 2Butanamine, 2Methyl1Propanamine, 2Methyl2Propanamine, Pyrrole, 1,2, and 3Methylpyrrole, Pyridine, 2,3, and 4Methylpyridine, Pyrrolidine, Piperidine, Indole, Quinoline, Isoquinoline, Acridine, Carbazole, Phenanthridine, 1 and 2Naphthalenamine, and 9Methylcarbazole (Journal of Physical and Chemical Reference Data, 1993)
- N-(2,6-Dimethoxypyridine-3-yl)-9-Methylcarbazole-3-Sulfonamide as a Novel Tubulin Ligand against Human Cancer (Clinical Cancer Research, 2008)
- Total synthesis of the cyclic monoterpenoid pyrano[3,2- a ]carbazole alkaloids derived from 2-hydroxy-6-methylcarbazole (Organic and Biomolecular Chemistry, 2014)
- Photophysics of a 2,7-dimethoxy-N-methylcarbazole-based polysiloxane (Macromolecules, 1993)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2=C(C=C1)C3=CC=CC=C3N2
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InChIKeyPWJYOTPKLOICJK-UHFFFAOYSA-N
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