7-Azidoheptanoic acid is an organic compound characterized by the presence of an azido group (-N3) and a carboxylic acid functional group (-COOH) within a seven-carbon aliphatic chain. This compound is notable for its potential applications in bioconjugation and as a building block in the synthesis of various bioactive molecules due to the reactivity of the azido group. The azido group can participate in click chemistry reactions, particularly with alkynes, facilitating the formation of stable triazole linkages. The presence of the carboxylic acid group imparts acidic properties, allowing for solubility in polar solvents and potential interactions with biological systems. Additionally, 7-azidoheptanoic acid may exhibit unique physical properties such as melting and boiling points influenced by its molecular structure and functional groups. Safety considerations are important when handling this compound, as azides can be sensitive and potentially explosive under certain conditions. Overall, 7-azidoheptanoic acid serves as a versatile compound in organic synthesis and materials science.

7-Azidoheptanoic acid

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7-Azido-heptanoic acid is an analog of the heptanoyl group. It has been shown to inhibit cancer cell growth and induce apoptosis in a variety of human tumor cells. This compound is used for the selective activation of anticancer drugs, as well as for the prevention of photodynamic damage to healthy tissue. 7-Azido-heptanoic acid can be conjugated with biomolecules such as proteins or peptides to form a bifunctional molecule that can function both as an acceptor and a donor. It also binds to streptavidin, which has been shown to have anticancer activity in mice.

CAS 135920-28-4: 7-Azidoheptanoic acid

7-Azido-heptanoic acid

Ref: 3D-FA73090

7-Azidoheptanoic acid

Ref: IN-DA009VTX