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Catalog Number:
15922
CAS Number:
959573-48-9
Boc-R)-γ-(4-nitrobenzyl)-L-proline
Purity:
98.60%
Documents
$72.31 /25MG
Pack Size Availability Price
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Product Information

Boc-(R)-g-(4-nitrobenzyl)-L-proline is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure, characterized by the presence of a 4-nitrobenzyl group, allows for selective modifications, facilitating the design of novel peptides with tailored biological activities.

This compound is particularly valuable in the synthesis of bioactive peptides and can be utilized in the development of therapeutic agents targeting various diseases. Its application extends to the pharmaceutical industry, where it aids in the creation of compounds with improved efficacy and reduced side effects. Researchers appreciate its ability to enhance solubility and bioavailability, making it a preferred choice for drug formulation. With its robust profile, Boc-(R)-g-(4-nitrobenzyl)-L-proline stands out as a key building block in the advancement of peptide-based therapeutics.

CAS Number
959573-48-9
Purity
98.60%
Molecular Formula
C17H22N2O6
Molecular Weight
350.37
MDL Number
MFCD06659415
PubChem ID
53398245
Conditions
Store at 0-8°C
General Information
CAS Number
959573-48-9
Purity
98.60%
Molecular Formula
C17H22N2O6
Molecular Weight
350.37
MDL Number
MFCD06659415
PubChem ID
53398245
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)-g-(4-nitrobenzyl)-L-proline 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 therapeutic agents. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it plays a critical role in designing new drugs, especially those targeting neurological disorders. The nitrobenzyl group can enhance the compound's bioactivity and selectivity.
  • Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to biomolecules for targeted drug delivery systems. This application is crucial in creating more effective treatments with reduced side effects.
  • Research in Organic Chemistry: It is frequently employed in organic synthesis as a versatile intermediate, allowing chemists to explore new reaction pathways and develop novel compounds.
  • Material Science: The compound finds applications in the development of smart materials, where its unique properties can be utilized to create responsive systems for various industrial applications.

Citations