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Catalog Number:
07274
CAS Number:
1214041-87-8
Boc-3,4-difluoro-DL-fenilalanina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-3,4-difluoro-DL-fenilalanina, Boc-3,4-difluoro-DL-Phe-OH, (Ácido RS -Boc-2-amino-3-(3,4-difluorofenil)propiónico
Documents
$103.56 /250 mg
Tamaño
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Product Information

Boc-3,4-difluoro-DL-phenylalanine is a versatile amino acid derivative that has garnered attention in pharmaceutical and biochemical research. This compound features a unique difluorophenyl group, which enhances its potential as a building block in the synthesis of novel peptides and drug candidates. Its protective Boc (tert-butyloxycarbonyl) group allows for selective deprotection, making it an ideal choice for researchers looking to develop complex molecules with precision. The incorporation of fluorine atoms can also improve the metabolic stability and bioavailability of therapeutic agents, providing a significant advantage in drug development.

In practical applications, Boc-3,4-difluoro-DL-phenylalanine is utilized in the synthesis of peptide-based drugs and in the study of protein interactions. Its unique properties enable researchers to explore new avenues in medicinal chemistry, particularly in the design of inhibitors and modulators for various biological targets. The compound's ability to enhance the pharmacological profile of peptides makes it a valuable asset in the quest for innovative therapeutic solutions.

Synonyms
Boc-3,4-difluoro-DL-fenilalanina, Boc-3,4-difluoro-DL-Phe-OH, (Ácido RS -Boc-2-amino-3-(3,4-difluorofenil)propiónico
CAS Number
1214041-87-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H17F2NO4
Molecular Weight
301.3
MDL Number
MFCD03788084
PubChem ID
2756792
Melting Point
103-110 ?C
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-3,4-difluoro-DL-fenilalanina, Boc-3,4-difluoro-DL-Phe-OH, (Ácido RS -Boc-2-amino-3-(3,4-difluorofenil)propiónico
CAS Number
1214041-87-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H17F2NO4
Molecular Weight
301.3
MDL Number
MFCD03788084
PubChem ID
2756792
Melting Point
103-110 ?C
Conditions
Conservar entre 0 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-3,4-difluoro-DL-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: Its unique fluorinated structure enhances the bioactivity and stability of drug candidates, making it valuable in the pharmaceutical industry for creating more effective treatments.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme activities, providing insights into metabolic pathways and disease mechanisms.
  • Diagnostic Applications: The compound can be incorporated into diagnostic agents, improving the sensitivity and specificity of tests used in medical diagnostics.
  • Material Science: Its properties are explored in the development of new materials, particularly in coatings and polymers, where enhanced chemical resistance is desired.

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