For research use only. Not for therapeutic Use.
N-Allylaniline(Cat No.:I014493) is a compound commonly used as a separation material or stationary phase in various chromatographic techniques, such as gas chromatography and liquid chromatography. It possesses the ability to interact selectively with different analytes based on their chemical properties, allowing for the separation and analysis of complex mixtures. N-Allylaniline’s chemical structure and functional groups enable it to exhibit specific interactions, such as hydrogen bonding and π-π interactions, contributing to its effectiveness as a separation material in chromatography applications.
Catalog Number | I014493 |
CAS Number | 589-09-3 |
Synonyms | N-Allylaniline; AI3-10028; AI3 10028; AI310028;Benzenamine, N-2-propenyl- |
Molecular Formula | C9H11N |
Purity | ≥95% |
Solubility | Soluble in DMSO |
IUPAC Name | N-prop-2-enylaniline |
InChI | InChI=1S/C9H11N/c1-2-8-10-9-6-4-3-5-7-9/h2-7,10H,1,8H2 |
InChIKey | LQFLWKPCQITJIH-UHFFFAOYSA-N |
SMILES | C=CCNC1=CC=CC=C1 |
Reference | </br> 1: Dana M, Luliński P, Maciejewska D. Synthesis of homoveratric acid-imprinted polymers and their evaluation as selective separation materials. Molecules. 2011 May 5;16(5):3826-44. doi: 10.3390/molecules16053826. PubMed PMID: 21546882.</br>2: Mossine VV, Barnes CL, Mawhinney TP. Disordered hydrogen bonding in N-(1-deoxy-beta-D-fructopyranos-1-yl)-N-allylaniline. Carbohydr Res. 2009 May 12;344(7):948-51. doi: 10.1016/j.carres.2009.02.017. Epub 2009 Feb 25. PubMed PMID: 19345935.</br>3: Leroi C, Bertin D, Dufils PE, Gigmes D, Marque S, Tordo P, Couturier JL, Guerret O, Ciufolini MA. Alkoxyamine-mediated radical synthesis of indoliNAs and indolines. Org Lett. 2003 Dec 25;5(26):4943-5. PubMed PMID: 14682735.</br>4: Inoue S, Takamatsu N, Kishi Y. [Synthetic studies on echinulin and realted natural products. I. Acid-catalyzed amino-Claisen rearrangement of N-allylaniline and N,N-diallylaniline derivatives (author’s transl)]. Yakugaku Zasshi. 1977 May;97(5):553-7. Japanese. PubMed PMID: 560461. </br> </br> |