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Catalog Number:
15483
CAS Number:
706806-75-9
Boc- R) -α-(4-bromobenzyl)proline
Purity:
≥ 99 % (HPLC)
Documents
$65.40 /100 mg
Taille
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Product Information

Boc-(R)-a-(4-bromobenzyl)proline is a valuable compound widely utilized in the synthesis of peptide-based pharmaceuticals and research applications. This compound features a unique bromobenzyl group that enhances its reactivity and selectivity, making it an excellent choice for researchers focusing on drug development and medicinal chemistry. Its Boc (tert-butyloxycarbonyl) protecting group allows for easy manipulation during synthesis, facilitating the formation of complex structures while maintaining stability under various conditions.

In the pharmaceutical industry, Boc-(R)-a-(4-bromobenzyl)proline serves as a crucial building block for the development of bioactive peptides, which are essential in therapeutic applications such as cancer treatment and pain management. Its ability to act as a chiral auxiliary also makes it a preferred choice for asymmetric synthesis, providing researchers with the means to create enantiomerically pure compounds. With its robust properties and versatility, this compound stands out as an essential tool for advancing research and development in the field of medicinal chemistry.

CAS Number
706806-75-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C 17 H 22 BrNO 4
Molecular Weight
384.27
MDL Number
MFCD06797550
PubChem ID
4279827
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +163 ± 2º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
General Information
CAS Number
706806-75-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C 17 H 22 BrNO 4
Molecular Weight
384.27
MDL Number
MFCD06797550
PubChem ID
4279827
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +163 ± 2º (C=1 dans MeOH)
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-(R)-a-(4-bromobenzyl)proline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of biologically active compounds. Its unique structure allows for the incorporation of specific functionalities that enhance peptide stability and activity.
  • Drug Development: The compound is valuable in medicinal chemistry for designing new pharmaceuticals, especially in the field of neuropharmacology. Its ability to mimic natural amino acids makes it a candidate for creating drugs targeting neurological disorders.
  • Research in Protein Engineering: It is used in the modification of proteins to study structure-function relationships. By incorporating this compound, researchers can explore how changes in amino acid sequences affect protein behavior.
  • Bioconjugation Applications: The compound can be employed in bioconjugation techniques, linking drugs or imaging agents to biomolecules. This enhances the specificity and efficacy of therapeutic agents in targeted drug delivery systems.
  • Development of Chiral Catalysts: Its chiral nature makes it suitable for creating asymmetric catalysts in organic synthesis, providing an advantage in producing enantiomerically pure compounds, which are crucial in pharmaceuticals.

Citations