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Catalog Number:
15658
CAS Number:
501015-32-3
Fmoc-(S)-3-amino-3-(3-hydroxyphenyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-β-Phe(3-OH)-OH, Fmoc-L-β-m-Tyr-OH
Documents
$206.60 /1G
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Product Information

Fmoc-(S)-3-amino-3-(3-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 crucial for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a hydroxyl group on the phenyl ring, enhances its reactivity and compatibility with various coupling reagents, making it an ideal choice for researchers focused on synthesizing complex peptides and biologically active compounds.

In pharmaceutical research, Fmoc-(S)-3-amino-3-(3-hydroxyphenyl)propionic acid has shown potential in the design of peptide-based therapeutics, particularly in targeting specific biological pathways. Its ability to facilitate the introduction of functional groups allows for the development of novel compounds with enhanced efficacy and specificity. This compound stands out for its stability and ease of use, providing researchers with a reliable tool for advancing their projects in medicinal chemistry and biochemistry.

Synonyms
Fmoc-L-β-Phe(3-OH)-OH, Fmoc-L-β-m-Tyr-OH
CAS Number
501015-32-3
Purity
≥ 98% (HPLC)
Molecular Formula
C24H21NO5
Molecular Weight
403.43
MDL Number
MFCD03427978
PubChem ID
24902255
Melting Point
160 - 162 °C
Appearance
White powder
Optical Rotation
[a]D25 = -28 ± 2 ° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-β-Phe(3-OH)-OH, Fmoc-L-β-m-Tyr-OH
CAS Number
501015-32-3
Purity
≥ 98% (HPLC)
Molecular Formula
C24H21NO5
Molecular Weight
403.43
MDL Number
MFCD03427978
PubChem ID
24902255
Melting Point
160 - 162 °C
Appearance
White powder
Optical Rotation
[a]D25 = -28 ± 2 ° (C=1 in DMF)
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

Fmoc-(S)-3-amino-3-(3-hydroxyphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in biochemistry.
  • Drug Development: The compound's structural features are beneficial in designing new pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, which is crucial in developing diagnostic tools and targeted drug delivery systems.
  • Research in Neuroscience: The compound's ability to mimic neurotransmitters makes it valuable in studying neurological pathways and developing treatments for neurodegenerative diseases.
  • Material Science: Its unique properties allow for the incorporation into polymer matrices, leading to the development of advanced materials with tailored functionalities for various applications.

Citations