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Catalog Number:
18498
CAS Number:
105751-19-7
Fmoc-DL-homoproline
Synonym(s):
Fmoc-DL-HomoPro-OH, Fmoc-DL-pipecolic acid
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Product Information

Fmoc-DL-homoproline is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which allows for selective deprotection during the synthesis process, making it an essential tool for chemists in the field of organic synthesis. Its unique structure enhances the stability and solubility of peptides, facilitating the formation of complex structures that are crucial in pharmaceutical research.

Researchers and industry professionals appreciate Fmoc-DL-homoproline for its ability to introduce homoproline residues into peptides, which can significantly influence the biological activity and stability of the resulting compounds. This characteristic is particularly beneficial in the design of peptide-based therapeutics and in the development of novel biomaterials. With its proven efficacy in enhancing peptide properties, Fmoc-DL-homoproline stands out as a valuable asset in both academic and industrial laboratories focused on peptide chemistry and drug discovery.

Synonyms
Fmoc-DL-HomoPro-OH, Fmoc-DL-pipecolic acid
CAS Number
105751-19-7
Molecular Formula
C21H21NO4
Molecular Weight
351.4
MDL Number
MFCD01823265
PubChem ID
3790985
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-DL-HomoPro-OH, Fmoc-DL-pipecolic acid
CAS Number
105751-19-7
Molecular Formula
C21H21NO4
Molecular Weight
351.4
MDL Number
MFCD01823265
PubChem ID
3790985
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-DL-homoproline 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 without affecting the overall structure.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds that can target specific biological pathways.
  • Bioconjugation: Fmoc-DL-homoproline is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors.
  • Research in Neuroscience: This compound is valuable in studying neuropeptides and their functions, contributing to advancements in understanding neurological disorders.
  • Material Science: It finds applications in creating functionalized polymers, enhancing material properties for various industrial applications, such as coatings and adhesives.

Citations