Beta-amino ketones
Beta-amino ketones are a class of organic compounds characterized by the presence of both an amino group (?NH?) and a ketone group (C=O) in the β-position relative to each other. These functional groups are typically located on the same carbon atom, although there can be variations depending on the specific compound structure.
Structurally, these compounds have a general formula R-C(R’)-C(=O)-NH? where R and R’ represent alkyl or aryl substituents. Beta-amino ketones are versatile intermediates in organic synthesis due to their reactivity and functional group diversity. They can participate in various reactions such as nucleophilic substitutions, condensation reactions, and coupling processes.
These compounds find applications in the pharmaceutical industry for synthesizing drugs with specific amino ketone structures, which often serve as key building blocks or are directly used as active pharmaceutical ingredients (APIs). Additionally, they are also utilized in agrochemicals, cosmetics, and other fine chemicals due to their unique properties.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2-Propanone,1-[(2R)-2-pyrrolidinyl]- | 130325-43-8 | C7H13NO |
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(+)-Ferruginine | 73069-63-3 | C10H15NO |
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1-(pyrrolidin-2-yl)propan-2-one | 71294-64-9 | C7H13NO |
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Ethanone, 1-(8-methyl-8-azabicyclo[3.2.1]oct-2-en-2-yl)- (9CI) | 137331-57-8 | C10H15NO |
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