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Catalog Number:
15261
CAS Number:
261165-06-4
Boc-(S)-3-amino-3-(4-bromophenyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-Phe(4-Br)-OH, (S)-Boc-4-Bromo-β-phenylalanine
Documents
$72.31 /250MG
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Product Information

Boc-(S)-3-amino-3-(4-bromophenyl)propionic acid is a valuable compound widely utilized in pharmaceutical research and development. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, enhancing its stability and facilitating its use in peptide synthesis. Its unique structure, characterized by the presence of a bromophenyl group, allows for specific interactions in biological systems, making it a crucial building block in the design of novel therapeutics. Researchers have leveraged this compound in the synthesis of bioactive peptides and small molecules, particularly in the development of targeted therapies for various diseases, including cancer and neurological disorders.

The compound's advantageous properties include its high purity and ease of handling, which are essential for laboratory applications. Its ability to undergo selective reactions makes it an ideal candidate for further functionalization, allowing chemists to explore diverse chemical pathways. With its significant role in advancing medicinal chemistry, Boc-(S)-3-amino-3-(4-bromophenyl)propionic acid stands out as a key ingredient for researchers aiming to innovate in drug discovery and development.

Synonyms
Boc-L-β-Phe(4-Br)-OH, (S)-Boc-4-Bromo-β-phenylalanine
CAS Number
261165-06-4
Purity
≥ 98% (HPLC)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD03419292
PubChem ID
2756775
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -46 ± 2 º (C=1 in CH3CO2H or EtOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-β-Phe(4-Br)-OH, (S)-Boc-4-Bromo-β-phenylalanine
CAS Number
261165-06-4
Purity
≥ 98% (HPLC)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD03419292
PubChem ID
2756775
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -46 ± 2 º (C=1 in CH3CO2H or EtOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-3-amino-3-(4-bromophenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders. Its unique structure allows for modifications that enhance bioactivity.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, providing a protective group that facilitates the assembly of complex peptides. This is crucial in developing peptide-based therapeutics.
  • Bioconjugation: The compound can be employed in bioconjugation processes, where it helps attach drugs to antibodies or other biomolecules, improving targeted delivery and efficacy in cancer therapies.
  • Research in Neuroscience: Its bromophenyl group makes it a valuable tool in studying receptor interactions and signaling pathways in the brain, aiding researchers in understanding various neurological conditions.
  • Material Science: The compound's unique properties allow it to be incorporated into polymers for creating advanced materials, which can be used in drug delivery systems or as scaffolds in tissue engineering.

Citations