Boc-p-azido-D-Phe-OH, also known as Boc-protected p-azido-D-phenylalanine, is a chemical compound commonly used in peptide synthesis and bioconjugation applications. It features a Boc (tert-butyloxycarbonyl) protecting group, which is often employed to protect amine functionalities during synthetic procedures. The presence of the azido group (-N3) allows for further functionalization through click chemistry, making it a valuable intermediate in the development of bioactive peptides and pharmaceuticals. The D-phenylalanine moiety contributes to the compound's structural and stereochemical properties, influencing its interactions in biological systems. Typically, this compound is characterized by its stability under standard laboratory conditions, although it should be handled with care due to the potential reactivity of the azido group. Its solubility is generally favorable in organic solvents, which facilitates its use in various synthetic protocols. Overall, Boc-p-azido-D-Phe-OH serves as a versatile building block in organic and medicinal chemistry, particularly in the context of peptide and drug design.

Boc-p-azido-D-Phe-OH

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CAS 214630-05-4: Boc-p-azido-D-Phe-OH

Boc-p-azido-D-Phe-OH

Ref: 54-OR36405

Boc-4-azido-D-phenylalanine

Ref: 3D-FB48516

Boc-4-azido-D-phenylalanine

Ref: 10-F492857

BOC-P-AZIDO-D-PHE-OH

Ref: IN-DA00BEUR