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Catalog Number:
47386
CAS Number:
144207-41-0
Ácido ( S )-Fmoc-2-amino-5,5,5-trifluoropentanoico
Purity:
≥ 99,5 % (HPLC quiral)
Synonym(s):
Ácido ( S )-2-((((9 H -Fluoren-9-il)metoxi)carbonil)amino)-5,5,5-trifluoropentanoico
Documents
$70.00 /25 mg
Tamaño
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Product Information

(S)-Fmoc-2-amino-5,5,5-trifluoropentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique trifluoromethyl group, enhancing its bioactivity and stability, making it an attractive choice for researchers focused on developing novel therapeutics. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides with high purity and yield.

In the pharmaceutical industry, (S)-Fmoc-2-amino-5,5,5-trifluoropentanoic acid is particularly valuable in the design of peptide-based drugs, where its trifluoromethyl moiety can significantly influence the pharmacokinetic properties of the resulting compounds. Additionally, its application extends to the development of biologically active molecules in medicinal chemistry, providing researchers with a powerful tool for creating innovative solutions in drug discovery. The compound's unique properties and ease of use make it an essential component for professionals looking to enhance their research and development efforts.

Synonyms
Ácido ( S )-2-((((9 H -Fluoren-9-il)metoxi)carbonil)amino)-5,5,5-trifluoropentanoico
CAS Number
144207-41-0
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C20H18F3NO4
Molecular Weight
393.36
MDL Number
MFCD31580021
PubChem ID
19107250
Appearance
Polvo blanco
Conditions
Tienda en RT
General Information
Synonyms
Ácido ( S )-2-((((9 H -Fluoren-9-il)metoxi)carbonil)amino)-5,5,5-trifluoropentanoico
CAS Number
144207-41-0
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C20H18F3NO4
Molecular Weight
393.36
MDL Number
MFCD31580021
PubChem ID
19107250
Appearance
Polvo blanco
Conditions
Tienda en RT
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-5,5,5-trifluoropentanoic 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), allowing for the incorporation of fluorinated amino acids that can enhance the stability and bioactivity of the resulting peptides.
  • Drug Development: Its unique trifluoromethyl group can improve the pharmacokinetic properties of drug candidates, making it valuable in pharmaceutical research for developing more effective therapeutics.
  • Bioconjugation: The Fmoc protecting group allows for selective reactions in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in the development of targeted drug delivery systems.
  • Material Science: This compound can be used in the creation of advanced materials, particularly in coatings or polymers that require enhanced chemical resistance and durability due to the presence of fluorine.
  • Research in Fluorine Chemistry: It provides a platform for exploring the effects of fluorination in various chemical reactions, helping researchers understand the role of fluorine in modifying biological and chemical properties.

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