| Weight | 121.183 g/mol |
|---|---|
| Formula | C8H11N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-Methylbenzylamine (100-81-2)
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- An enantioselective approach to (+)-thienamycin from dimethyl 1,3-acetonedicarboxylate and (+)-.alpha.-methylbenzylamine (Journal of Organic Chemistry, 1986)
- Halide-Bridged Palladium(II) Dimers of Orthometalated (S)-(+)-N,N-Dimethyl--methylbenzylamine and (S)-(+)-N,N-Dimethyl[1-(2-naphthyl)ethyl]amine: Solution and Solid-State Structures and Reactions with 3,4-Dimethyl-1-phenylphosphole and Allyldiphenylphosphine (Organometallics, 2000)
- Inhibition of phenylethanolamine N-methyltransferase by benzylamines. 2. In vitro and in vivo studies with 2,3-dichloro- -methylbenzylamine. (Journal of Medicinal Chemistry, 1973)
- Mechanistic switch leading to highly efficient chirality transfer in Pd(0)-catalyzed couplingcyclization of aryl iodides with 11 acidbase salts of 2,3-allenoic acids and l-()-cinchonidine or d-(+)-/l-()--methylbenzylamine. Enantioselective synthesis of highly optically active 3-aryl polysubstituted butenolidesElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b1/b109645a/ (Chemical Communications, 2002)
- Asymmetric Pictet-Spengler reaction with chiral-N-(-3-indoly)ethyl-1-methylbenzylamine (Tetrahedron Letters, 1995)
- Radioiodinated N -[3-(4-morpholino)propyl]- N -methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9): a new potential melanoma imaging agent (European Journal of Nuclear Medicine and Molecular Imaging, 2001)
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SMILESCC1=CC(=CC=C1)CN
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InChIKeyRGXUCUWVGKLACF-UHFFFAOYSA-N
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