| Weight | 121.183 g/mol |
|---|---|
| Formula | C8H11N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
N-Methyl-o-toluidine (611-21-2)
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- Structure-mutagenicity relationships of N-oxidized derivatives of aniline, o-toluidine, 2'-methyl-4-aminobiphenyl, and 3,2'-dimethyl-4-aminobiphenyl. (Journal of Medicinal Chemistry, 1979)
- Carbon dioxide: a reagent for the simultaneous protection of nucleophilic centers and the activation of alternative locations to electrophilic attack. 17. Substitution of N-methyl-1- and N-methyl-2-naphthylamine and side-chain functionalization of o-toluidine (Journal of Organic Chemistry, 1991)
- Poly (N-methyl pyrrole) and its copolymer with o-toluidine electrodeposited on steel in mixture of DBSA and oxalic acid electrolytes (Current Applied Physics, 2011)
- Carbon dioxide : a reagent for the simultaneous protection of nucleophilic centers and the activation of alternative locations to electrophilic attack. XVI, A novel synthetic method for the side-chain functionalization of N-methyl-o-toluidine and for the preparation of 2-substituted N-methylindoles (Heterocycles, 1990)
- Rearrangement of N-Triphenylmethyl-o-toluidine. Direct Synthesis of 3-Methyl-4-aminophenyltriphenylmethane (Journal of the American Chemical Society, 1941)
- A PRACTICAL SYNTHETIC METHOD FOR N-METHYL-o-TOLUIDINE (Organic Preparations and Procedures International, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H412: Harmful to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 3 -
SMILESCC1=CC=CC=C1NC
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InChIKeyGUAWMXYQZKVRCW-UHFFFAOYSA-N
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