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Catalog Number:
15884
CAS Number:
144085-23-4
Boc-R)-a-allylproline
Purity:
≥ 98% (NMR)
Documents
$113.87 /100MG
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Product Information

Boc-(R)-a-allylproline is a valuable compound widely utilized in the field of organic synthesis and medicinal chemistry. This amino acid derivative features a unique allyl group that enhances its reactivity and versatility, making it an essential building block for the synthesis of various bioactive molecules. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, facilitating the development of complex peptide structures and other organic compounds. Researchers and industry professionals appreciate its role in the design of novel pharmaceuticals, particularly in the development of inhibitors and modulators for various biological targets.

The compound's distinct properties, such as its ability to participate in asymmetric synthesis, make it particularly advantageous for creating enantiomerically pure products. This characteristic is crucial in the pharmaceutical industry, where the efficacy and safety of drugs can be significantly influenced by their stereochemistry. Boc-(R)-a-allylproline has been effectively employed in the synthesis of peptide-based therapeutics and can serve as a precursor for more complex structures, showcasing its potential in advancing drug discovery and development.

CAS Number
144085-23-4
Purity
≥ 98% (NMR)
Molecular Formula
C13H21NO4
Molecular Weight
255.31
MDL Number
MFCD01076221
PubChem ID
4607339
Appearance
Off white powder
Conditions
Store at 0-8°C
General Information
CAS Number
144085-23-4
Purity
≥ 98% (NMR)
Molecular Formula
C13H21NO4
Molecular Weight
255.31
MDL Number
MFCD01076221
PubChem ID
4607339
Appearance
Off white powder
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

Boc-(R)-a-allylproline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating cyclic peptides that can have enhanced biological activity.
  • Drug Development: Its unique structure allows for the design of novel pharmaceuticals, especially in the development of drugs targeting neurological disorders, due to its ability to mimic natural amino acids.
  • Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Organocatalysis: Boc-(R)-a-allylproline is employed as an organocatalyst in various organic reactions, providing an environmentally friendly alternative to traditional metal catalysts.
  • Studying Protein Interactions: It is used in research to investigate protein-ligand interactions, helping scientists understand how proteins function and how they can be targeted for therapeutic purposes.

Citations