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Catalog Number:
05135
CAS Number:
26250-84-0
Boc-L-homoproline
Purity:
≥ 99 % (HPLC chirale, HPLC)
Synonym(s):
Boc-L-HomoPro-OH, Acide (S)-1-Boc-pipéridine-2-carboxylique
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$29.34 /5G
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Product Information

Boc-L-homoproline is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for the synthesis of complex peptides and proteins. Its unique structure allows for the incorporation of homoproline into peptides, which can influence the biological activity and stability of the resulting compounds. Researchers have found that Boc-L-homoproline can be particularly beneficial in the development of peptide-based therapeutics, as it can improve the conformational properties of peptides and enhance their interaction with biological targets.

In addition to its applications in drug development, Boc-L-homoproline serves as a building block in the synthesis of various bioactive molecules. Its ability to mimic natural amino acids while providing distinct properties makes it a versatile tool in medicinal chemistry. The compound is also used in the study of protein folding and structure, offering insights into the design of novel biomolecules. With its robust profile and practical applications, Boc-L-homoproline is an essential resource for researchers and industry professionals looking to innovate in the fields of biochemistry and pharmaceuticals.

Synonyms
Boc-L-HomoPro-OH, Acide (S)-1-Boc-pipéridine-2-carboxylique
CAS Number
26250-84-0
Purity
≥ 99 % (HPLC chirale, HPLC)
Molecular Formula
C 11 H 19 NON 4
Molecular Weight
229.3
MDL Number
MFCD00151904
PubChem ID
581831
Melting Point
122 - 126 ºC
Appearance
Poudre cristalline blanc cassé ou blanche
Optical Rotation
[a] D 20 = -62 à -64 º (C=1 dans CH 3 COOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-HomoPro-OH, Acide (S)-1-Boc-pipéridine-2-carboxylique
CAS Number
26250-84-0
Purity
≥ 99 % (HPLC chirale, HPLC)
Molecular Formula
C 11 H 19 NON 4
Molecular Weight
229.3
MDL Number
MFCD00151904
PubChem ID
581831
Melting Point
122 - 126 ºC
Appearance
Poudre cristalline blanc cassé ou blanche
Optical Rotation
[a] D 20 = -62 à -64 º (C=1 dans CH 3 COOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-L-homoproline is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of cyclic peptides that exhibit enhanced stability and biological activity.
  • Drug Development: Its unique structure allows for the modification of peptide drugs, improving their pharmacokinetics and therapeutic efficacy, which is crucial in pharmaceutical research.
  • Bioconjugation: Boc-L-homoproline is used in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules, facilitating targeted drug delivery systems.
  • Research in Neuroscience: This compound is explored in studies related to neurotransmitter systems, aiding in the understanding of neurological disorders and the development of potential treatments.
  • Material Science: It finds applications in creating novel materials with specific properties, such as hydrogels, which can be used in drug delivery and tissue engineering.

Citations