Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
15567
CAS Number:
500770-76-3
Ácido Boc-( S -3-amino-3-(3-bromofenil)propiónico
Purity:
≥ 99% (HPLC, pureza quiral)
Synonym(s):
Boc-L-β-Phe(3-Br)-OH, ( S -Boc-3-bromo-β-fenilalanina
Documents
$72.31 /250 mg
Tamaño
Request Bulk Quote
Product Information

Boc-(S)-3-amino-3-(3-bromophenyl)propionic acid is a versatile building block in organic synthesis, particularly valued in the pharmaceutical and biotechnology sectors. This compound features a unique bromophenyl group, which enhances its reactivity and allows for the development of novel therapeutic agents. Its Boc (tert-butyloxycarbonyl) protecting group facilitates easy manipulation during peptide synthesis, making it an essential intermediate for researchers focused on drug development and peptide chemistry.

This compound has shown potential in the synthesis of bioactive molecules, including those targeting neurological disorders and cancer. Its ability to serve as a chiral auxiliary also opens avenues for asymmetric synthesis, providing researchers with a reliable tool for creating enantiomerically pure compounds. With its favorable properties and applications, Boc-(S)-3-amino-3-(3-bromophenyl)propionic acid stands out as a valuable asset for professionals in medicinal chemistry and related fields.

Synonyms
Boc-L-β-Phe(3-Br)-OH, ( S -Boc-3-bromo-β-fenilalanina
CAS Number
500770-76-3
Purity
≥ 99% (HPLC, pureza quiral)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD03427924
PubChem ID
2764535
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-β-Phe(3-Br)-OH, ( S -Boc-3-bromo-β-fenilalanina
CAS Number
500770-76-3
Purity
≥ 99% (HPLC, pureza quiral)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD03427924
PubChem ID
2764535
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a versatile building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it helps create biologically active compounds.
  • Drug Development: It plays a crucial role in the development of new drugs, especially those targeting neurological disorders, due to its ability to modify amino acid structures effectively.
  • Bioconjugation: The compound is used in bioconjugation processes to attach drugs or imaging agents to biomolecules, enhancing the specificity and efficacy of therapeutic agents.
  • Research in Neuroscience: Its unique structure allows researchers to study receptor interactions and signaling pathways, contributing to advancements in understanding brain function and disorders.
  • Custom Synthesis: Many laboratories utilize this compound for custom synthesis projects, providing tailored solutions for specific research needs in medicinal chemistry.

Citas