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Catalog Number:
29699
CAS Number:
1219145-37-5
Ácido R , S -Fmoc-2-amino-4,4,4-trifluorobutírico
Purity:
≥ 98 % (HPLC)
Documents
$86.23 /25 mg
Tamaño
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Product Information

(R,S)-Fmoc-2-amino-4,4,4-trifluoro-butyric acid is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its trifluoromethyl group enhances the compound's stability and lipophilicity, making it particularly valuable in the development of biologically active peptides and drug candidates. Researchers appreciate its ability to facilitate the formation of complex peptide structures while maintaining high purity and yield.

In addition to its role in peptide synthesis, (R,S)-Fmoc-2-amino-4,4,4-trifluoro-butyric acid is also employed in the design of novel therapeutic agents, especially in the fields of oncology and neurology. Its unique properties allow for the exploration of new drug formulations that can target specific biological pathways. With its combination of stability, reactivity, and ease of use, this compound stands out as a crucial tool for researchers aiming to innovate in drug development and peptide chemistry.

CAS Number
1219145-37-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 19 H 16 F 3 NO 4
Molecular Weight
379.34
MDL Number
MFCD02682447
PubChem ID
46737291
Melting Point
189-193 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1219145-37-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 19 H 16 F 3 NO 4
Molecular Weight
379.34
MDL Number
MFCD02682447
PubChem ID
46737291
Melting Point
189-193 ?C
Appearance
Polvo blanco
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

(R,S)-Fmoc-2-amino-4,4,4-trifluoro-butyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids while preventing unwanted reactions.
  • Drug Development: Its unique trifluoromethyl group enhances the pharmacological properties of peptides, making it valuable in the design of more effective therapeutic agents.
  • Bioconjugation: The compound can be employed in bioconjugation techniques, facilitating the attachment of peptides to other biomolecules or surfaces for targeted drug delivery applications.
  • Research in Fluorinated Compounds: Its fluorinated structure allows researchers to study the effects of fluorination on biological activity, providing insights into drug design and optimization.
  • Analytical Chemistry: This chemical serves as a standard in analytical methods, helping to calibrate instruments and validate procedures for peptide analysis.

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