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

Catalog Number:
12792
CAS Number:
352351-61-2
Fmoc-2,4-dicloro-D-fenilalanina
Purity:
≥ 98%
Synonym(s):
Fmoc-D-Phe(2,4-DiCl)-OH, Fmoc-D-Phe(2,4- Cl2 )-OH
Documents
$89.13 /1G
Tamaño
Request Bulk Quote
Product Information

Fmoc-2,4-dichloro-D-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective coupling of amino acids during solid-phase peptide synthesis. Its structure, characterized by the presence of two chlorine atoms on the phenyl ring, enhances its reactivity and allows for the introduction of diverse functionalities in peptide sequences. Researchers appreciate its role in creating peptides with specific biological activities, making it invaluable in pharmaceutical research and development.

In addition to its applications in peptide synthesis, Fmoc-2,4-dichloro-D-phenylalanine is also explored for its potential in designing novel therapeutics targeting various diseases. Its unique properties enable chemists to develop compounds with improved efficacy and selectivity. This compound stands out among similar derivatives due to its enhanced stability and reactivity, making it a preferred choice for professionals seeking reliable building blocks in their synthetic pathways.

Synonyms
Fmoc-D-Phe(2,4-DiCl)-OH, Fmoc-D-Phe(2,4- Cl2 )-OH
CAS Number
352351-61-2
Purity
≥ 98%
Molecular Formula
C24H19Cl2NO4
Molecular Weight
456.4
MDL Number
MFCD01863047
PubChem ID
3349164
Melting Point
156-162 ?C
Appearance
Polvo amorfo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Phe(2,4-DiCl)-OH, Fmoc-D-Phe(2,4- Cl2 )-OH
CAS Number
352351-61-2
Purity
≥ 98%
Molecular Formula
C24H19Cl2NO4
Molecular Weight
456.4
MDL Number
MFCD01863047
PubChem ID
3349164
Melting Point
156-162 ?C
Appearance
Polvo amorfo 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

Fmoc-2,4-dichloro-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures with high purity and yield.
  • Drug Development: Its unique properties make it valuable in pharmaceutical research, especially in developing new therapeutic agents targeting specific diseases, including cancer and metabolic disorders.
  • Bioconjugation: The chemical is used in bioconjugation processes, where it helps attach biomolecules to drugs or imaging agents, enhancing their efficacy and targeting capabilities in medical applications.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, aiding researchers in understanding the mechanisms of action for various neurological disorders and potential treatments.
  • Custom Synthesis: Laboratories often utilize this compound for custom synthesis projects, allowing researchers to tailor-make compounds for specific experimental needs, thus accelerating innovation in chemical research.

Citas