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Catalog Number:
15661
CAS Number:
501015-33-4
Acide Fmoc-(S)-3-amino-3-(4-hydroxyphényl)propionique
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc-L-β-Phe(4-OH)-OH, Fmoc-L-β-Tyr-OH
Documents
$72.31 /100 mg
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Product Information

Fmoc-(S)-3-amino-3-(4-hydroxyphenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, characterized by the presence of a 4-hydroxyphenyl group, enhances its reactivity and compatibility with various coupling reagents, making it an ideal choice for researchers focused on developing complex peptide sequences.

In the pharmaceutical industry, this compound plays a crucial role in the design of bioactive peptides, which can lead to the discovery of new therapeutic agents. Its application extends to the fields of biochemistry and molecular biology, where it is employed in the synthesis of peptide-based probes and therapeutics. Researchers appreciate its stability and ease of use, which facilitate efficient synthesis processes. With its significant potential in advancing peptide chemistry, Fmoc-(S)-3-amino-3-(4-hydroxyphenyl)propionic acid stands out as a valuable asset for professionals aiming to innovate in drug design and development.

Synonyms
Fmoc-L-β-Phe(4-OH)-OH, Fmoc-L-β-Tyr-OH
CAS Number
501015-33-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD03427979
PubChem ID
24902256
Melting Point
165 - 171 ?C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -38 ± 1 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-β-Phe(4-OH)-OH, Fmoc-L-β-Tyr-OH
CAS Number
501015-33-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD03427979
PubChem ID
24902256
Melting Point
165 - 171 ?C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -38 ± 1 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(4-hydroxyphenyl)propionic 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, allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the functionality of diagnostic tools and drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter pathways, aiding researchers in understanding the role of amino acids in brain function and potential treatments for neurological disorders.
  • Material Science: The compound is also explored in the development of novel materials, particularly in creating polymers with specific properties for applications in coatings and electronics.

Citations