Boc-(S)-3-amino-5-hexenoic acid is a chemical compound characterized by its structure, which includes a Boc (tert-butyloxycarbonyl) protecting group attached to the amino group of an amino acid derivative. This compound features a hexenoic acid backbone, indicating the presence of a double bond within a six-carbon chain, which contributes to its reactivity and potential applications in organic synthesis. The "S" designation indicates that the compound has a specific stereochemistry, which is crucial for its biological activity and interactions. The Boc group serves as a protective moiety, allowing for selective reactions at other functional groups without interference from the amino group. This compound is often utilized in peptide synthesis and medicinal chemistry, where the controlled release of the amino group is advantageous. Its unique structural features make it a valuable intermediate in the development of pharmaceuticals and biologically active molecules. As with many amino acid derivatives, it may exhibit properties such as solubility in polar solvents and potential for forming hydrogen bonds, influencing its behavior in various chemical environments.

Boc-(S)-3-amino-5-hexenoic acid

270263-03-1: Boc-(R)-3-amino-5-hexenoic acid, (3S)-3-[(tert-butoxycarbonyl)amino]hex-5-enoic acid, Boc-β-HoGly(Allyl)-OH

(S)-3-((tert-Butoxycarbonyl)amino)hex-5-enoic acid

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CAS 270263-03-1: Boc-(S)-3-amino-5-hexenoic acid

(S)-3-((tert-Butoxycarbonyl)amino)hex-5-enoic acid

Ref: IN-DA003OF2

(S)-3-((tert-Butoxycarbonyl)amino)hex-5-enoic acid

Ref: 10-F237195

(S)-3-((tert-Butoxycarbonyl)amino)hex-5-enoic acid

Ref: 54-OR83472

Boc-L-β-homoallylglycine

Ref: 3D-FB50183

(S)-3-(Boc-amino)-5-hexenoic acid

Ref: 7W-GM3633