Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
15760
CAS Number:
1217662-71-9
Boc-(S-α-(3-bromobenzyl)proline
Purity:
≥ 97% (HPLC)
Documents
$84.83 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-(S)-a-(3-bromobenzyl)proline is a versatile compound widely utilized in the field of medicinal chemistry and pharmaceutical research. This amino acid derivative, characterized by its unique bromobenzyl group, serves as a crucial building block in the synthesis of various bioactive molecules. Its ability to enhance the solubility and stability of peptide-based drugs makes it particularly valuable in drug development processes. Researchers have leveraged this compound in the design of potent inhibitors and therapeutic agents, especially in the realms of cancer and neurological disorders.

The compound's distinctive properties, including its chiral nature and protective Boc (tert-butyloxycarbonyl) group, facilitate its incorporation into complex molecular architectures. This enables chemists to explore diverse modifications and functionalizations, ultimately leading to the discovery of novel therapeutic candidates. With its proven track record in enhancing drug efficacy and safety profiles, Boc-(S)-a-(3-bromobenzyl)proline stands out as an essential tool for researchers aiming to innovate in drug design and development.

CAS Number
1217662-71-9
Purity
≥ 97% (HPLC)
Molecular Formula
C17H22BrNO4
Molecular Weight
384.27
MDL Number
MFCD06796765
PubChem ID
53398114
Appearance
White powder
Optical Rotation
[a]D25 = -94 ± 2º (C=1 in EtOH) or
Conditions
Store at 0-8 °C
General Information
CAS Number
1217662-71-9
Purity
≥ 97% (HPLC)
Molecular Formula
C17H22BrNO4
Molecular Weight
384.27
MDL Number
MFCD06796765
PubChem ID
53398114
Appearance
White powder
Optical Rotation
[a]D25 = -94 ± 2º (C=1 in EtOH) or
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-a-(3-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 creation of peptides with specific functionalities.
  • Drug Development: Researchers leverage this chemical in the design of new pharmaceuticals, especially in the field of cancer research, where it can be used to create targeted therapies that interact with specific cellular pathways.
  • Bioconjugation: It is employed in bioconjugation techniques, linking biomolecules to therapeutic agents, enhancing the efficacy and specificity of drug delivery systems.
  • Protein Engineering: The compound is useful in modifying proteins to improve their stability and activity, which is essential for developing more effective biopharmaceuticals.
  • Research in Neuroscience: Its application extends to neuroscience, where it aids in the study of neuropeptides and their role in neurological disorders, providing insights that could lead to innovative treatments.

Citations