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Catalog Number:
15886
CAS Number:
706806-59-9
Boc-(S-α-allylproline
Purity:
≥ 98% (NMR)
Synonym(s):
(S-2-Allyl-1-Boc-2-pyrrolidinecarboxylic acid, (S-2-Allyl-pyrrolidine-1,2-dicarboxylic acid1-tert-butyl ester
Documents
$208.31 /100MG
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Product Information

Boc-(S)-a-allylproline is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. Its unique structure, featuring a tert-butoxycarbonyl (Boc) protecting group, enhances its stability and solubility, making it an ideal choice for researchers in organic chemistry and pharmaceutical applications. This compound is particularly valuable in the synthesis of cyclic peptides and as a building block for creating bioactive molecules, which are essential in medicinal chemistry.

In addition to its applications in peptide synthesis, Boc-(S)-a-allylproline is also utilized in the development of novel therapeutic agents, particularly in the fields of oncology and neurology. Its ability to facilitate the formation of complex molecular architectures allows for the exploration of new drug candidates with improved efficacy and selectivity. Researchers appreciate its compatibility with various coupling reagents and reaction conditions, making it a reliable choice for diverse synthetic pathways. With its significant potential in advancing drug discovery and development, Boc-(S)-a-allylproline stands out as a key compound for professionals in the chemical and pharmaceutical industries.

Synonyms
(S-2-Allyl-1-Boc-2-pyrrolidinecarboxylic acid, (S-2-Allyl-pyrrolidine-1,2-dicarboxylic acid1-tert-butyl ester
CAS Number
706806-59-9
Purity
≥ 98% (NMR)
Molecular Formula
C13H21NO4
Molecular Weight
255.31
MDL Number
MFCD06659382
PubChem ID
4607339
Appearance
Off-white powder
Conditions
Store at 0-8°C
General Information
Synonyms
(S-2-Allyl-1-Boc-2-pyrrolidinecarboxylic acid, (S-2-Allyl-pyrrolidine-1,2-dicarboxylic acid1-tert-butyl ester
CAS Number
706806-59-9
Purity
≥ 98% (NMR)
Molecular Formula
C13H21NO4
Molecular Weight
255.31
MDL Number
MFCD06659382
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-(S)-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 the creation of cyclic peptides that are important in drug discovery.
  • Drug Development: Its unique structure allows for the design of novel pharmaceuticals, especially in the development of compounds targeting neurological disorders.
  • Chiral Catalysis: The compound is used in asymmetric synthesis, providing an efficient method for producing chiral molecules, which are essential in the pharmaceutical industry.
  • Bioconjugation: Boc-(S)-a-allylproline can be utilized in bioconjugation techniques, aiding in the attachment of biomolecules to surfaces or other molecules for enhanced drug delivery systems.
  • Research in Organic Chemistry: It serves as a key intermediate in various organic reactions, facilitating the study of reaction mechanisms and the development of new synthetic methodologies.

Citations