BOC-L-2-amino-4-bromo-4-pentenoic acid, with the CAS number 151215-34-8, is a synthetic amino acid derivative characterized by the presence of a bromine atom and a pentenoic acid structure. This compound features a tert-butyloxycarbonyl (BOC) protecting group on the amino group, which is commonly used in peptide synthesis to protect the amine functionality during chemical reactions. The presence of the bromo substituent introduces unique reactivity, making it useful in various organic synthesis applications. The pentenoic acid moiety contributes to its potential as a building block in the synthesis of more complex molecules, particularly in the field of medicinal chemistry. This compound is typically handled with care due to its reactivity and potential biological activity. Its solubility and stability can vary depending on the solvent and conditions, which are important considerations for its use in laboratory settings. Overall, BOC-L-2-amino-4-bromo-4-pentenoic acid serves as a valuable intermediate in the development of pharmaceuticals and other chemical products.

BOC-L-2-AMINO-4-BROMO-4-PENTENOIC ACID

151215-34-8: (S)-N-Boc-(2-Bromoallyl)-Glycine

4-Pentenoic acid, 4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-

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CAS 151215-34-8: BOC-L-2-AMINO-4-BROMO-4-PENTENOIC ACID

4-Pentenoic acid, 4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-

Ref: IN-DA001N6P

Boc-L-2-amino-4-bromo-4-pentenoic acid

Ref: 3D-FB50628

(S)-4-Bromo-2-((tert-butoxycarbonyl)amino)pent-4-enoic acid

Ref: 10-F241374