Weight | 131.178 g/mol |
---|---|
Formula | C9H9N |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
7-Methylindole (933-67-5)
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- Metal template reactions. XX. Macrocyclic metal complexes derived from 4,6-Dimethoxy-3-methylindole-2,7-dicarbaldehyde and some primary diamines with additional nitrogen donor atoms (Australian Journal of Chemistry, 1983)
- Regioselective lithiation and substitution of tricarbonyl-(6-1-methylindole)-chromium(0) : X-ray crystal structure analysis of tricarbonyl-(6-1-methyl-2-trimethylsilyl-7-ethoxycarbonyl-indole)chromium(0) (Journal of The Chemical Society, Chemical Communications, 1981)
- 3-Substituted-5-aziridinyl-1-methylindole-4,7-diones as NQO1-directed antitumour agents: mechanism of activation and cytotoxicity in vitro (Biochemical Pharmacology, 2003)
- Synthesis of 5-Methylindole-4,7-quinone Through a New Construction of the Functionalized Indole Ring Based on the Allene-Mediated Electrocyclic Reaction Involving the Pyrrole[b]-Bond. (Heterocycles, 2004)
- Synthetic studies on mitomycin. I: Synthesis of 7-methoxymitosene from 6-methylindole by selective oxidation of benzene part (Heterocycles, 1987)
- The use of 7-methylindole in the antimony trichloride colour test for vitamin A (Biochemical Journal, 1932)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=CC2=C1NC=C2
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InChIKeyKGWPHCDTOLQQEP-UHFFFAOYSA-N
- Pubchem - 7-Methylindole
- Wikipedia - 7-methylindole
7-Methylindole is a mildly toxic off-white crystalline organic compound with chemical formula C9H9N. It is used in the production of agricultural chemicals and pharmaceuticals.
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