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Catalog Number:
15219
CAS Number:
151911-33-0
S-3-Amino-3-(4-fluorophenyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
L-β-Phe(4-F)-OH, (S-4-Fluoro-β-phenylalanine
Documents
$72.31 /250MG
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Product Information

(S)-3-Amino-3-(4-fluorophenyl)propionic acid is a valuable compound in the field of pharmaceutical research and development. This amino acid derivative, known for its unique structural features, serves as a potent building block in the synthesis of various bioactive molecules. Its fluorinated phenyl group enhances its pharmacological properties, making it a key candidate in the design of novel therapeutics, particularly in the treatment of neurological disorders. Researchers have utilized this compound in studies aimed at understanding receptor interactions and developing targeted therapies, showcasing its relevance in medicinal chemistry.

Additionally, (S)-3-Amino-3-(4-fluorophenyl)propionic acid demonstrates excellent solubility and stability, which are critical for formulation in drug development. Its ability to modulate neurotransmitter activity positions it as a promising agent in neuropharmacology. The compound's unique characteristics not only facilitate innovative research but also offer significant advantages over similar compounds, making it an essential choice for professionals in the pharmaceutical industry seeking to advance their projects.

Synonyms
L-β-Phe(4-F)-OH, (S-4-Fluoro-β-phenylalanine
CAS Number
151911-33-0
Purity
≥ 98% (HPLC)
Molecular Formula
C9H10FNO2
Molecular Weight
183.0
MDL Number
MFCD03840458
PubChem ID
579885
Appearance
Off-white to pale yellow powder
Conditions
Store at 0-8°C
General Information
Synonyms
L-β-Phe(4-F)-OH, (S-4-Fluoro-β-phenylalanine
CAS Number
151911-33-0
Purity
≥ 98% (HPLC)
Molecular Formula
C9H10FNO2
Molecular Weight
183.0
MDL Number
MFCD03840458
PubChem ID
579885
Appearance
Off-white to pale yellow powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-3-Amino-3-(4-fluorophenyl)propionic acid is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in developing drugs targeting neurological disorders. Its structural properties allow for modifications that enhance therapeutic efficacy.
  • Neurotransmitter Research: It plays a significant role in studies related to neurotransmitter systems, especially in understanding the mechanisms of excitatory neurotransmission. Researchers can explore its effects on synaptic plasticity and cognitive functions.
  • Biochemical Assays: The compound is used in biochemical assays to evaluate the activity of enzymes and receptors. Its specificity can help in screening potential drug candidates and understanding their interactions at a molecular level.
  • Material Science: In material science, it can be incorporated into polymers to enhance their properties, such as thermal stability and mechanical strength, making it valuable in developing advanced materials for various applications.
  • Academic Research: It is frequently employed in academic research settings to investigate the effects of amino acid derivatives on biological systems, contributing to a deeper understanding of metabolic pathways and cellular functions.

Citations