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Catalog Number:
47387
CAS Number:
2230472-61-2
Ácido (S)-Fmoc-2-amino-6,6,6-trifluorohexanoico
Purity:
≥ 99,5 % (HPLC quiral)
Synonym(s):
Ácido ( S )-2-((((9 H -Fluoren-9-il)metoxi)carbonil)amino)-6,6,6-trifluorohexanoico
Documents
$90.00 /25 mg
Tamaño
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Product Information

(S)-Fmoc-2-amino-6,6,6-trifluorohexanoic acid is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique trifluoromethyl group, which enhances its bioactivity and stability, making it an ideal choice for researchers focused on developing fluorinated peptides. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy manipulation during synthesis, providing a robust platform for the construction of complex peptide structures.

In practical applications, (S)-Fmoc-2-amino-6,6,6-trifluorohexanoic acid is particularly valuable in the pharmaceutical industry for the design of peptide-based therapeutics, where fluorinated amino acids can improve pharmacokinetic properties. Its ability to introduce fluorine into peptide sequences can lead to enhanced binding affinity and selectivity, making it a crucial component in the development of novel drugs. Researchers appreciate its versatility and effectiveness in producing high-quality peptides, which are essential for various applications, including vaccine development and targeted therapies.

Synonyms
Ácido ( S )-2-((((9 H -Fluoren-9-il)metoxi)carbonil)amino)-6,6,6-trifluorohexanoico
CAS Number
2230472-61-2
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C21H20F3NO4
Molecular Weight
407.38
MDL Number
MFCD32696662
PubChem ID
103694688
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido ( S )-2-((((9 H -Fluoren-9-il)metoxi)carbonil)amino)-6,6,6-trifluorohexanoico
CAS Number
2230472-61-2
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C21H20F3NO4
Molecular Weight
407.38
MDL Number
MFCD32696662
PubChem ID
103694688
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

(S)-Fmoc-2-amino-6,6,6-trifluorohexanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), where its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for easy removal during the synthesis process.
  • Drug Development: Its unique trifluoromethyl group enhances the pharmacokinetic properties of peptides, making it valuable in the design of novel therapeutics with improved efficacy and stability.
  • Bioconjugation: The compound can be used in bioconjugation techniques, allowing for the attachment of peptides to various biomolecules, which is crucial in developing targeted drug delivery systems.
  • Research in Fluorinated Compounds: It provides insights into the behavior of fluorinated amino acids in biological systems, aiding researchers in understanding the effects of fluorination on protein structure and function.
  • Custom Peptide Libraries: This chemical is instrumental in creating diverse peptide libraries for screening in drug discovery, enabling researchers to identify potential leads more efficiently.

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