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

Catalog Number:
15562
CAS Number:
500770-75-2
Acide boc-( S -3-amino-3-(2-bromophényl)propionique)
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-L-β-Phe(2-Br)-OH, ( S -Boc-2-bromo-β-phénylalanine
Documents
$79.22 /250 mg
Taille
Request Bulk Quote
Product Information

Boc-(S)-3-amino-3-(2-bromophenyl)propionic acid is a valuable compound widely utilized in pharmaceutical research and development. This amino acid derivative features a unique bromophenyl group, which enhances its reactivity and potential applications in the synthesis of biologically active molecules. Its Boc (tert-butyloxycarbonyl) protecting group allows for easy manipulation in peptide synthesis, making it an essential building block for researchers working on drug discovery and development.

This compound is particularly relevant in the field of medicinal chemistry, where it can be employed in the design of novel therapeutic agents targeting various diseases. Its structural characteristics lend themselves to the development of compounds with improved efficacy and selectivity. Additionally, Boc-(S)-3-amino-3-(2-bromophenyl)propionic acid can be used in the synthesis of peptide-based drugs, providing researchers with a versatile tool for exploring new therapeutic pathways. Its ability to facilitate complex chemical reactions while maintaining stability makes it a preferred choice among professionals in the industry.

Synonyms
Boc-L-β-Phe(2-Br)-OH, ( S -Boc-2-bromo-β-phénylalanine
CAS Number
500770-75-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD03427923
PubChem ID
3744756
Melting Point
141-149 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +21 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(2-Br)-OH, ( S -Boc-2-bromo-β-phénylalanine
CAS Number
500770-75-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD03427923
PubChem ID
3744756
Melting Point
141-149 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +21 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(S)-3-amino-3-(2-bromophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry where custom peptides are developed for drug discovery.
  • Drug Development: Its unique structure allows researchers to explore new therapeutic agents, especially in the field of cancer research, where it can be used to develop targeted treatments.
  • Biochemical Research: The compound is valuable in studying enzyme interactions and protein functions, aiding researchers in understanding biological mechanisms at a molecular level.
  • Material Science: It can be incorporated into polymers and materials, enhancing properties such as thermal stability and mechanical strength, which is beneficial for developing advanced materials.
  • Analytical Chemistry: This chemical is used as a standard in various analytical techniques, helping to calibrate instruments and ensure accurate measurements in research laboratories.

Citations