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Catalog Number:
16835
CAS Number:
749847-57-2
L-2,4,5-Trifluorophénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
( S -2,4,5-Trifluorophénylalanine
Documents
$30.00 /100 mg
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Product Information

L-2,4,5-Trifluorophenylalanine is a unique amino acid derivative that has garnered attention in various fields, particularly in pharmaceutical and biochemical research. This compound, characterized by its trifluorophenyl group, offers distinct properties that enhance its utility in the development of novel therapeutics and research applications. Its structural modifications allow for increased stability and specificity in protein interactions, making it a valuable tool for researchers investigating protein folding, enzyme activity, and receptor binding.

In the pharmaceutical industry, L-2,4,5-Trifluorophenylalanine is being explored for its potential role in drug design, particularly in the synthesis of fluorinated compounds that exhibit improved bioavailability and metabolic stability. Additionally, its unique fluorine atoms can be leveraged in imaging studies, providing insights into biological processes at the molecular level. Researchers and industry professionals can benefit from incorporating this compound into their studies, as it opens avenues for innovative solutions in drug discovery and development.

Synonyms
( S -2,4,5-Trifluorophénylalanine
CAS Number
749847-57-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 9 H 8 F 3 NON 2
Molecular Weight
219.16
MDL Number
MFCD06657675
PubChem ID
5003427
Melting Point
230 - 235 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a]D25 = -1.2 ±0.5 (C=1.96 in water)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( S -2,4,5-Trifluorophénylalanine
CAS Number
749847-57-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 9 H 8 F 3 NON 2
Molecular Weight
219.16
MDL Number
MFCD06657675
PubChem ID
5003427
Melting Point
230 - 235 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a]D25 = -1.2 ±0.5 (C=1.96 in water)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

L-2,4,5-Trifluorophenylalanine is widely utilized in research focused on:

  • Drug Development: This compound serves as a valuable building block in the synthesis of novel pharmaceuticals, particularly in the design of drugs targeting specific neurological disorders due to its unique fluorinated structure.
  • Biochemistry Research: It is used in studies to understand protein folding and function, as the trifluoromethyl group can influence the interactions within proteins, providing insights into enzyme activity and stability.
  • Material Science: The compound is explored in the development of advanced materials, including polymers and coatings, where its properties can enhance thermal stability and chemical resistance.
  • Fluorine Chemistry: As a fluorinated amino acid, it is instrumental in fluorine chemistry research, helping scientists investigate the effects of fluorine substitution on biological activity and molecular interactions.
  • Analytical Chemistry: It is utilized in analytical methods to improve the detection and quantification of biomolecules, leveraging its distinct spectral properties for better sensitivity in assays.

Citations