Aralkylamines
Aralkylamines are a class of organic compounds characterized by the presence of an amino group (-NH?) attached to an aromatic ring substituted with one or more alkyl groups. These compounds find applications in various industries due to their diverse chemical properties and reactivity. In pharmaceuticals, aralkylamines are used as intermediates for the synthesis of drugs with specific biological activities, such as antihistamines and antidepressants. Their ability to form stable complexes with metals makes them valuable in catalyst systems and chelating agents. Additionally, these compounds play a significant role in the production of surfactants, dyes, and agrochemicals. The unique structure of aralkylamines allows for their modification through various synthetic routes, enabling the development of new functional materials and products with enhanced performance characteristics.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2-Isopropylamino-1-phenyl-ethanolHydrochloride | 10568-00-0 | C11H18ClNO |
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a-2-(Methylamino)ethylbenzyl Alcohol | 42142-52-9 | C10H15NO |
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pyrimidin-4-ylmethanamine | 45588-79-2 | C5H7N3 |
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DL-Phenylglycinol | 7568-92-5 | C8H11NO |
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3-(2-Chlorophenyl)aminopropanenitrile | 94-89-3 | C9H9ClN2 |
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3-Anilinopropionitrile | 1075-76-9 | C9H10N2 |
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N1-phenylethane-1,2-diamine | 1664-40-0 | C8H12N2 |
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(1R)-2-amino-1-phenylethan-1-ol | 2549-14-6 | C8H11NO |
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4-(1H-Imidazol-4-yl)-1-methylpiperidine | 106243-44-1 | C9H15N3 |
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N-Methyl-2-thiopheneethanamine | 106891-32-1 | C7H11NS |
Related Literature
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