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Catalog Number:
33595
CAS Number:
1213887-81-0
Boc-2-cloro-4-fluoro-L-fenilalanina
Synonym(s):
Boc-L-Fe(2-Cl,4-F)-OH, (Ácido S -Boc-2-amino-2-cloro-4-fluorofenilpropiónico, Boc-Fe(2-Cl,4-F)-OH
Documents
$58.39 /100 mg
Tamaño
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Product Information

Boc-2-chloro-4-fluoro-L-phenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a unique combination of a Boc (tert-butyloxycarbonyl) protecting group and a 2-chloro-4-fluorophenyl side chain, which enhances its reactivity and selectivity in various chemical reactions. Researchers appreciate its role in the development of biologically active peptides and its potential applications in drug discovery, particularly in the design of inhibitors and modulators for therapeutic targets.

The compound's distinct properties make it an excellent choice for creating complex peptide structures, allowing for the exploration of new therapeutic avenues in fields such as oncology and neurology. Its stability and compatibility with standard coupling reagents further facilitate its incorporation into diverse synthetic pathways. With its growing relevance in medicinal chemistry, Boc-2-chloro-4-fluoro-L-phenylalanine stands out as a crucial building block for innovative research and development projects.

Synonyms
Boc-L-Fe(2-Cl,4-F)-OH, (Ácido S -Boc-2-amino-2-cloro-4-fluorofenilpropiónico, Boc-Fe(2-Cl,4-F)-OH
CAS Number
1213887-81-0
Molecular Formula
C14H17ClFNO4
Molecular Weight
317.74
MDL Number
MFCD12198162
PubChem ID
53398085
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Boc-L-Fe(2-Cl,4-F)-OH, (Ácido S -Boc-2-amino-2-cloro-4-fluorofenilpropiónico, Boc-Fe(2-Cl,4-F)-OH
CAS Number
1213887-81-0
Molecular Formula
C14H17ClFNO4
Molecular Weight
317.74
MDL Number
MFCD12198162
PubChem ID
53398085
Conditions
Conservar entre 2 y 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-2-chloro-4-fluoro-L-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 the development of pharmaceuticals that target specific biological pathways.
  • Drug Development: It is used in the design of novel drugs, especially in cancer therapy, where modifying amino acids can enhance drug efficacy and specificity.
  • Bioconjugation: The chemical's unique properties allow for effective bioconjugation, facilitating the attachment of drugs to antibodies for targeted therapy, improving treatment outcomes.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, helping researchers understand the effects of modified amino acids on brain function and behavior.
  • Analytical Chemistry: This compound is utilized in analytical methods to quantify amino acids in biological samples, aiding in metabolic studies and nutritional assessments.

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