| Weight | 131.178 g/mol |
|---|---|
| Formula | C9H9N |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
5-METHYLINDOLE (614-96-0)
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- Crystal and molecular structure of an antiinflammatory agent, indomethacin, 1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid (Journal of the American Chemical Society, 1972)
- A biosynthetic approach to the structure of eumelanins. The isolation of oligomers from 5,6-dihydroxy-1-methylindole. (Tetrahedron, 1986)
- The inhibitory effect of 5-acetoxy-2-(4-acetoxyphenyl)-1-ethyl-3-methylindole (D 16726) on estrogen-dependent mammary tumors (European Journal of Cancer and Clinical Oncology, 1985)
- Glycerides as prodrugs. 3. Synthesis and antiinflammatory activity of [1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetyl]glycerides (indomethacin glycerides). (Journal of Medicinal Chemistry, 1980)
- Electrosyntheses of high quality poly(5-methylindole) films in mixed electrolytes of boron trifluoride diethyl etherate and diethyl ether (European Polymer Journal, 2006)
- Melanin. 2. Electrochemical study of the oxidation of .alpha.-methyldopa and 5,6-dihydroxy-2-methylindole (Journal of Organic Chemistry, 1980)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2=C(C=C1)NC=C2
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InChIKeyYPKBCLZFIYBSHK-UHFFFAOYSA-N
- Pubchem - 5-METHYLINDOLE
- Wikipedia - 5-methylindole
5-Methylindole is an irritating organic compound with chemical formula C9H9N. 5-Methylindole is used as an intermediate in the synthesis of compounds with a variety of pharmacological properties, such as staurosporine-like bisindole inhibitors of protein kinases.
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5-METHYLINDOLE
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