| Weight | 133.194 g/mol |
|---|---|
| Formula | C9H11N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
N-Allylaniline (589-09-3)
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- Sigma-Aldrich - N-Allylaniline54.40 USD
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- Palladium-catalyzed synthesis of N-aryl-2-benzylindolines via tandem arylation of 2-allylaniline: control of selectivity through in situ catalyst modification. (Journal of the American Chemical Society, 2004)
- Metal complexes with allylanilines : IV. Synthesis and reactivity of rhodium(I) complexes with 2-allylaniline and N-allylaniline (Journal of Organometallic Chemistry, 1980)
- Evidence for the AminoClaisen rearrangement occurring in the molecular ions of N-allylaniline (Journal of Mass Spectrometry, 1986)
- The gasphase aminoclaisen rearrangement of protonated Nallylaniline (Journal of Mass Spectrometry, 1988)
- Conversion of N-allylaniline promoted by Rh(I): synthesis and molecular structure of 2-ethyl-1,2,3,4-tetrahydro-3-methyl-4-anilinoquinoline (Organometallics, 1988)
- Metal Complexes with Allylanilines. II. Rearrangement of the Ligands N-Allylaniline, N,N-Allylmethylaniline, 2-Allylaniline Promoted by Co-ordination to Pd(II) and Pt(II) (Synthesis and Reactivity in Inorganic and Metal-organic Chemistry, 1979)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC=CCNC1=CC=CC=C1
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InChIKeyLQFLWKPCQITJIH-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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N-Allylaniline
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