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Catalog Number:
15904
CAS Number:
959576-35-3
Boc- R) -γ-(4-clorobencil)-L-prolina
Purity:
≥ 98%
Documents
$93.14 /100 mg
Tamaño
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Product Information

Boc-(R)-g-(4-chlorobenzyl)-L-proline is a versatile amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers focused on developing complex peptides and biologically active molecules. Its unique structure, characterized by the presence of a 4-chlorobenzyl group, allows for specific interactions in biological systems, which can be leveraged in drug design and development.

In the pharmaceutical industry, Boc-(R)-g-(4-chlorobenzyl)-L-proline is particularly valuable for its application in the synthesis of peptide-based therapeutics. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid structure makes it a preferred choice among chemists. Additionally, its compatibility with various coupling reagents and reaction conditions enhances its utility in diverse synthetic pathways. Researchers can benefit from its use in creating targeted therapies, particularly in oncology and neurology, where peptide-based drugs are gaining traction.

CAS Number
959576-35-3
Purity
≥ 98%
Molecular Formula
C17H22ClNO4
Molecular Weight
339.82
MDL Number
MFCD06659397
PubChem ID
53398221
Melting Point
130 - 136 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -15,5 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
959576-35-3
Purity
≥ 98%
Molecular Formula
C17H22ClNO4
Molecular Weight
339.82
MDL Number
MFCD06659397
PubChem ID
53398221
Melting Point
130 - 136 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -15,5 ± 2 º (C=1 en DMF)
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-chlorobenzyl)-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 pharmaceutical agents. Its unique structure allows for the introduction of specific functional groups that enhance biological activity.
  • Drug Development: In medicinal chemistry, it is used to create proline derivatives that may exhibit improved efficacy and reduced side effects in drug formulations, particularly in treatments targeting neurological disorders.
  • Bioconjugation: The compound can be employed in bioconjugation processes, where it helps link biomolecules to therapeutic agents, improving the delivery and targeting of drugs in cancer therapy.
  • Research in Enzyme Inhibition: It is utilized in studies aimed at understanding enzyme mechanisms, particularly in the context of designing inhibitors that can modulate enzyme activity for therapeutic purposes.
  • Custom Synthesis: Researchers in academia and industry use this compound for custom synthesis projects, allowing for the creation of tailored molecules that meet specific research needs or therapeutic targets.

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