N-BOC-L- phenyl alanine

Also known as N-(tert-Butoxycarbonyl)-L-phenylalanine, N-t-Butyloxycarbonyl-L-phenylalanine, N-tert-Butyloxycarbonyl-L-phenylalanine

CAS number
13734-34-4
Molecular formula
C14H19NO4
Molecular weight
265.31 g/mol
Catalogue number
OS-11946
Purity
99 %
Form
Powder
Packing
25 kg

₹900 per kg

Specifications

Identity
CAS number 13734-34-4
Molecular formula C14H19NO4
Molecular weight 265.31 g/mol
IUPAC name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid
InChIKey ZYJPUMXJBDHSIF-NSHDSACASA-N
SMILES CC(C)(C)OC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O
MDL number MFCD00002663
PubChem CID 77857
Physical properties
Physical form Powder
Quality
Purity 99 %
Packaging
Packaging size 25 kg

Description

Synonym(s):Boc-L-Phe-OH, (S-2-tert-Butoxycarbonylamino-3-phenylpropionicacid Boc-L-phenylalanine is widely utilized in research focused on:
  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceuticals, Boc-L-phenylalanine is used to create peptide-based drugs. Its incorporation can enhance the bioactivity and stability of therapeutic peptides, making them more effective in treating diseases.
  • Biotechnology: Researchers in biotechnology utilize this compound for the production of modified proteins. By incorporating Boc-L-phenylalanine, scientists can study protein interactions and functions more effectively.
  • Analytical Chemistry: It is employed in various analytical techniques, including chromatography, to separate and identify amino acids and peptides. This application is crucial for quality control in food and pharmaceutical industries.
  • Research in Neuroscience: The compound is used in studies related to neurotransmitter

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