| Weight | 131.178 g/mol |
|---|---|
| Formula | C9H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1-METHYLINDOLE (603-76-9)
1-methylindole monopicrate
Score:
#2168 in Physics
,
#6718 in Chemistry
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LabBot
- 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)
- Infrared and Ultraviolet Spectroscopy of Water-Containing Clusters of Indole, 1-Methylindole, and 3-Methylindole (Journal of Physical Chemistry A, 1999)
- [-(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)
- CAN- and Iodine-Catalyzed Reaction of Indole or 1-Methylindole with ,-Unsaturated Ketone or Aldehyde. (Tetrahedron Letters, 2006)
- Inhibition of 3-methylindole bioactivation by the cytochrome P-450 suicide substrates 1-aminobenzotriazole and alpha-methylbenzylaminobenzotriazole. (Drug Metabolism and Disposition, 1989)
- A biosynthetic approach to the structure of eumelanins. The isolation of oligomers from 5,6-dihydroxy-1-methylindole. (Tetrahedron, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-methylindole monopicrate
-
SMILESCN1C=CC2=CC=CC=C21
-
InChIKeyBLRHMMGNCXNXJL-UHFFFAOYSA-N
- Pubchem - 1-METHYLINDOLE
- Wikipedia - 1-methylindole
1-Methylindole is an irritating, potentially toxic organic compound which occurs as a deep yellow viscous liquid with a very strong unpleasant odor. It has the chemical formula C9H9N.
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1-METHYLINDOLE
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