CAS 114117-42-9: BOC-PHE(4-NHAC)-OH

Description: BOC-PHE(4-NHAC)-OH, also known by its CAS number 114117-42-9, is a chemical compound that features a protected phenylalanine derivative. The "BOC" (tert-butyloxycarbonyl) group serves as a protective moiety for the amino group, which is commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. The "4-NHAC" indicates the presence of an acetamido group at the para position of the phenyl ring, which can influence the compound's solubility and reactivity. This compound is typically utilized in the synthesis of peptides and other bioactive molecules, where the protection of functional groups is crucial for achieving desired chemical transformations. Its structure allows for specific interactions in biological systems, making it relevant in medicinal chemistry and drug development. The stability of the BOC group under certain conditions and its ability to be selectively removed make it a valuable tool in organic synthesis. Overall, BOC-PHE(4-NHAC)-OH is significant in the field of peptide chemistry and related applications.

Formula: C₁₆H₂₂N₂O₅

Synonyms:

• N-Alpha-T-Butoxycarbonyl-4-Acetamido-L-Phenylalanine
• (S)-N-Alpha-T-Butyloxycarbonyl-4-Acetylaminophenylalanine
• Boc-4-(Acetyl-Amino)-L-Phenylalanine
• Boc-S-Phe-(4-Nhac)-Oh
• Boc-L-Phe(4-Nh-Ac)

L-Phenylalanine, 4-(acetylamino)-N-[(1,1-dimethylethoxy)carbonyl]-

CAS: 114117-42-9

• Formula: C₁₆H₂₂N₂O₅
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 322.3563

(S)-3-(4-Acetamidophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid

CAS: 114117-42-9

• Purity: 95.0%
• Color and Shape: Solid
• Molecular weight: 322.3609924316406

Boc-4-(acetyl-amino)-L-phenylalanine

CAS: 114117-42-9

Please enquire for more information about Boc-4-(acetyl-amino)-L-phenylalanine including the price, delivery time and more detailed …

• Formula: C₁₆H₂₂N₂O₅
• Purity: Min. 95%
• Molecular weight: 322.36 g/mol