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Catalog Number:
15312
CAS Number:
269726-77-4
Boc-4-trifluorométhyl-D-β-homophénylalanine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Boc-D-β-HomoPhe(4-CF3)-OH, Acide Boc-( R -3-amino-4-(4-trifluorométhylphényl)butyrique
Documents
$80.00 /100 mg
Taille
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Product Information

Boc-4-trifluoromethyl-D-b-homophenylalanine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the pharmaceutical industry for its unique trifluoromethyl group, which enhances the lipophilicity and metabolic stability of peptides. Researchers utilize Boc-4-trifluoromethyl-D-b-homophenylalanine in the design of potent inhibitors and therapeutic agents, especially in the development of treatments for various diseases, including cancer and metabolic disorders. Its ability to improve the pharmacokinetic properties of peptides makes it an essential building block for medicinal chemists.

In addition to its applications in drug discovery, this compound is also employed in the synthesis of complex organic molecules, where its protective Boc group facilitates selective reactions. The trifluoromethyl moiety not only contributes to the compound's unique properties but also provides an advantage over similar compounds by enhancing binding affinity and selectivity in biological systems. With its diverse applications and significant benefits, Boc-4-trifluoromethyl-D-b-homophenylalanine is an invaluable asset for researchers and industry professionals alike.

Synonyms
Boc-D-β-HomoPhe(4-CF3)-OH, Acide Boc-( R -3-amino-4-(4-trifluorométhylphényl)butyrique
CAS Number
269726-77-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 16 H 20 F 3 NON 4
Molecular Weight
347.33
MDL Number
MFCD01860972
PubChem ID
53397970
Melting Point
133-139 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 15 ± 1 º (C = 1 dans MeOH)
Conditions
Conserver à 0-8 °C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
General Information
Synonyms
Boc-D-β-HomoPhe(4-CF3)-OH, Acide Boc-( R -3-amino-4-(4-trifluorométhylphényl)butyrique
CAS Number
269726-77-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 16 H 20 F 3 NON 4
Molecular Weight
347.33
MDL Number
MFCD01860972
PubChem ID
53397970
Melting Point
133-139 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 15 ± 1 º (C = 1 dans MeOH)
Conditions
Conserver à 0-8 °C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Properties
Additional property information coming soon!
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Applications

Boc-4-trifluoromethyl-D-b-homophenylalanine 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 therapeutic agents targeting specific biological pathways.
  • Drug Development: Its unique trifluoromethyl group enhances the pharmacological properties of drug candidates, making it valuable in medicinal chemistry for creating more effective pharmaceuticals.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving their specificity and efficacy in targeted therapies.
  • Research in Neuroscience: It is applied in studies exploring neurological functions and disorders, aiding in the design of compounds that can modulate neurotransmitter systems.
  • Material Science: The chemical's properties make it suitable for developing novel materials with specific functionalities, such as sensors or drug delivery systems, enhancing their performance in various applications.

Citations