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

Catalog Number:
15976
CAS Number:
959581-01-2
Boc- R) -γ-(4-piridinilmetil)-L-prolina
Purity:
≥ 99 % (HPLC)
Documents
$120.88 /25 mg
Tamaño
Request Bulk Quote
Product Information

Boc-(R)-g-(4-pyridinylmethyl)-L-proline is a versatile compound widely utilized in the field of medicinal chemistry and peptide synthesis. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers focused on drug development and synthesis. Its unique structure, characterized by the presence of a pyridine ring, allows for specific interactions in biological systems, facilitating the design of targeted therapies and novel pharmaceuticals.

In practical applications, Boc-(R)-g-(4-pyridinylmethyl)-L-proline serves as a key building block in the synthesis of bioactive peptides and small molecules. Its ability to form stable linkages with other amino acids and functional groups makes it invaluable in the development of peptide-based drugs, particularly in oncology and neurology. Researchers appreciate its ease of use and compatibility with various coupling reagents, which streamlines the synthesis process. The compound's favorable properties and potential for diverse applications position it as a significant asset in the toolkit of chemists and pharmaceutical developers.

CAS Number
959581-01-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C16H22N2O4
Molecular Weight
306.36
MDL Number
MFCD06659248
PubChem ID
53398320
Melting Point
195-201 ?C
Appearance
Sólido blanco
Optical Rotation
[a] D 25 = -8,8 ± 2º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
959581-01-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C16H22N2O4
Molecular Weight
306.36
MDL Number
MFCD06659248
PubChem ID
53398320
Melting Point
195-201 ?C
Appearance
Sólido blanco
Optical Rotation
[a] D 25 = -8,8 ± 2º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(R)-g-(4-pyridinylmethyl)-L-proline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, especially in the development of pharmaceuticals that target specific biological pathways.
  • Drug Development: It is used in the design of novel drug candidates, particularly in the field of cancer research, where it helps in creating compounds that can inhibit tumor growth effectively.
  • Bioconjugation: The chemical can be employed in bioconjugation processes, allowing researchers to attach biomolecules to drugs, enhancing their targeting capabilities and reducing side effects.
  • Research in Neuroscience: Its unique structure makes it valuable in studying neurotransmitter systems, aiding in the development of treatments for neurological disorders.
  • Material Science: The compound can be incorporated into polymers to create materials with specific properties, such as improved biocompatibility for medical devices.

Citas