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Catalog Number:
15376
CAS Number:
270065-74-2
Boc-2-trifluorometil-L-β-homofenilalanina
Purity:
≥ 98%
Synonym(s):
Boc-L-β-HomoPhe(2-CF3)-OH, Ácido Boc-( S -3-amino-4-(2-trifluorometilfenil)butírico
Documents
$106.96 /100 mg
Tamaño
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Product Information

Boc-2-trifluoromethyl-L-b-homophenylalanine is a specialized amino acid derivative that has garnered attention in the fields of medicinal chemistry and peptide synthesis. This compound features a unique trifluoromethyl group, which enhances its biological activity and stability, making it an ideal candidate for the development of novel therapeutics. Its Boc (tert-butyloxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex peptides with improved pharmacological properties.

Researchers and industry professionals can leverage Boc-2-trifluoromethyl-L-b-homophenylalanine in the design of peptide-based drugs, particularly in targeting specific receptors or pathways in disease models. Its distinctive properties enable the creation of more potent and selective compounds, which can lead to advancements in drug discovery and development. The trifluoromethyl moiety not only enhances lipophilicity but also contributes to the compound's metabolic stability, making it a valuable asset in pharmaceutical research and development.

Synonyms
Boc-L-β-HomoPhe(2-CF3)-OH, Ácido Boc-( S -3-amino-4-(2-trifluorometilfenil)butírico
CAS Number
270065-74-2
Purity
≥ 98%
Molecular Formula
C16H20F3NO4
Molecular Weight
347.33
MDL Number
MFCD01861064
PubChem ID
53397948
Melting Point
137-143 ?C
Appearance
Polvo blanco
Optical Rotation
[α] D 25 = -43 ± 2º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-β-HomoPhe(2-CF3)-OH, Ácido Boc-( S -3-amino-4-(2-trifluorometilfenil)butírico
CAS Number
270065-74-2
Purity
≥ 98%
Molecular Formula
C16H20F3NO4
Molecular Weight
347.33
MDL Number
MFCD01861064
PubChem ID
53397948
Melting Point
137-143 ?C
Appearance
Polvo blanco
Optical Rotation
[α] D 25 = -43 ± 2º (C=1 en EtOH)
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-2-trifluoromethyl-L-b-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of novel therapeutic agents.
  • Drug Development: Its unique trifluoromethyl group enhances the pharmacological properties of drug candidates, making it a key component in medicinal chemistry.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme activities, providing insights into biological processes.
  • Material Science: It can be incorporated into polymers to improve their thermal and mechanical properties, benefiting industries focused on advanced materials.
  • Fluorinated Compounds: The trifluoromethyl group imparts unique characteristics, making it useful in creating compounds with enhanced stability and bioactivity.

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