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Catalog Number:
15401
CAS Number:
270263-04-2
Fmoc-L-β-homoalilglicina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-β-HomoGly(alil)-OH, Ácido Fmoc-( S -3-amino-5-hexenoico
Documents
$141.41 /100 mg
Tamaño
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Product Information

Fmoc-L-b-homoallylglycine is a versatile amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. Renowned for its unique structural properties, this compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which facilitates the selective modification of amino acids during solid-phase peptide synthesis. Its homoallyl side chain enhances the compound's reactivity, making it an excellent choice for creating complex peptides with specific functionalities. Researchers appreciate its ability to introduce structural diversity into peptide libraries, which is crucial for drug discovery and development.

This compound is particularly valuable in the synthesis of bioactive peptides and can be employed in various applications, including the development of peptide-based therapeutics and probes for biological studies. Its stability under standard reaction conditions and compatibility with various coupling reagents further underscore its utility in synthetic chemistry. By incorporating Fmoc-L-b-homoallylglycine into your research, you can enhance the efficiency and effectiveness of your peptide synthesis projects, paving the way for innovative solutions in pharmaceutical development.

Synonyms
Fmoc-L-β-HomoGly(alil)-OH, Ácido Fmoc-( S -3-amino-5-hexenoico
CAS Number
270263-04-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C21H21Nº 4
Molecular Weight
351.4
MDL Number
MFCD01861088
PubChem ID
25178072
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = +17,0 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-β-HomoGly(alil)-OH, Ácido Fmoc-( S -3-amino-5-hexenoico
CAS Number
270263-04-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C21H21Nº 4
Molecular Weight
351.4
MDL Number
MFCD01861088
PubChem ID
25178072
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = +17,0 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 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-L-b-homoallylglycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in designing compounds that target specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter systems, helping scientists understand the role of specific amino acids in neural signaling.
  • Customizable Therapeutics: The versatility of this compound allows for modifications that can enhance the efficacy and specificity of therapeutic agents, making it a preferred choice in personalized medicine.

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