| Weight | 131.178 g/mol |
|---|---|
| Formula | C9H9N |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
2-METHYLINDOLE (95-20-5)
2-methylindole sodium salt
Score:
#2034 in Physics
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#6338 in Chemistry
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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)
- Oxidation of tryptophan and N-methylindole by N3.cntdot., Br2.-, and (SCN)2.- radicals in light- and heavy-water solutions: a pulse radiolysis study (The Journal of Physical Chemistry, 1991)
- Cyclizative Condensations. I. 2-Methylindole with Acetone and Methyl Ethyl Ketone1 (Journal of Organic Chemistry, 1961)
- [-(Dimethylamino)benzyllithiumDiethyl Ether]2, (S)--(Methylpivaloylamino)benzyllithium ()-Sparteine, and [3-Iodo-2-lithio-1-methylindole 2 Tetrahydrofuran]2: Crystal Structure Investigations of -Lithiated Amines (Chemische Berichte, 1993)
- Preparation of .beta.-substituted tryptophan derivatives: comparison of the reactivity of N-methylindole toward aziridine-2-lactones and aziridine-2-carboxylic esters and interpretation of results using MNDO calculations (Journal of Organic Chemistry, 1994)
- Evidence supporting the formation of 2,3-epoxy-3-methylindoline: a reactive intermediate of the pneumotoxin 3-methylindole. (Chemical Research in Toxicology, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-methylindole sodium salt
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SMILESCC1=CC2=CC=CC=C2N1
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InChIKeyBHNHHSOHWZKFOX-UHFFFAOYSA-N
- Pubchem - 2-METHYLINDOLE
- Wikipedia - 2-methylindole
Methylketol or 2-methylindole is a mildly toxic and slightly flammable organic compound which occurs as a white solid which turns brown over time. It has chemical formula C9H9N. Methylketol is used as an intermediate for synthesizing dyes, pigments, optical brighteners, and pharmaceuticals.
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