102507-18-6 | (2R, 3S)/(2S, 3R)-Racemic boc-beta-hydroxyphenylalanine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$137.00	$96.00
5g	97%	in stock	$541.00	$379.00
10g	97%	in stock	$1,030.00	$721.00
25g	97%	in stock	$1,901.00	$1,331.00

Description

• Catalog Number: AA09669
• Chemical Name: (2R, 3S)/(2S, 3R)-Racemic boc-beta-hydroxyphenylalanine
• CAS Number: 102507-18-6
• Molecular Formula: C14H19NO5
• Molecular Weight: 281.3044
• MDL Number: MFCD06656444
• SMILES: O=C(OC(C)(C)C)N[C@H]([C@H](c1ccccc1)O)C(=O)O

Upstream Synthesis Route

The compound rel-(βS)-N-[(1,1-Dimethylethoxy)carbonyl]-β-hydroxy-D-phenylalanine, also known as $name$, is a versatile building block in chemical synthesis. With its unique structure and functional groups, this compound is commonly used in peptide synthesis and pharmaceutical research.In chemical synthesis, rel-(βS)-N-[(1,1-Dimethylethoxy)carbonyl]-β-hydroxy-D-phenylalanine serves as a key intermediate for the creation of complex peptides and peptidomimetics. Its β-hydroxy-D-phenylalanine moiety allows for selective functionalization and modification, making it an essential component in designing novel peptide analogs with improved bioactivity and pharmacokinetic properties.Moreover, the presence of the N-[(1,1-Dimethylethoxy)carbonyl] protecting group ensures the stability of the compound during various synthetic steps, facilitating efficient peptide assembly and modification. By strategically incorporating this compound into synthesis routes, chemists can access a diverse array of peptide derivatives for structure-activity relationship studies, drug development, and biochemical research.Overall, the application of rel-(βS)-N-[(1,1-Dimethylethoxy)carbonyl]-β-hydroxy-D-phenylalanine in chemical synthesis enables the construction of sophisticated peptide structures with tailored functionalities and enhanced biological properties. Its versatile nature and compatibility with peptide chemistry make it a valuable tool for advancing the field of medicinal chemistry and biochemical research.