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Catalog Number:
05460
CAS Number:
172702-58-8
Boc-L-aspartic acid β-benzyl ester chloromethylketone
Purity:
99%
Synonym(s):
Boc-L-Asp(OBzl)-CMK
Documents
$756.93 /100MG
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Product Information

Boc-L-aspartic acid b-benzyl ester chloromethylketone is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This compound features a unique chloromethylketone functional group, which enhances its reactivity and makes it an excellent building block for the development of bioactive peptides. Its protective Boc (tert-butyloxycarbonyl) group allows for selective deprotection, facilitating the synthesis of complex peptide structures. Researchers appreciate its application in the design of inhibitors and drug candidates, particularly in the fields of oncology and neurology, where aspartic acid derivatives play a crucial role in modulating biological activity.

The compound's stability and ease of handling make it a preferred choice for chemists looking to streamline their synthesis processes. Additionally, its ability to undergo various chemical transformations opens up avenues for creating novel compounds with tailored properties. Whether you are involved in academic research or industrial applications, Boc-L-aspartic acid b-benzyl ester chloromethylketone offers significant advantages in efficiency and versatility, making it an essential addition to your chemical toolkit.

Synonyms
Boc-L-Asp(OBzl)-CMK
CAS Number
172702-58-8
Purity
99%
Molecular Formula
C17H22NO5Cl
Molecular Weight
355.82
MDL Number
MFCD00672491
PubChem ID
16760350
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Asp(OBzl)-CMK
CAS Number
172702-58-8
Purity
99%
Molecular Formula
C17H22NO5Cl
Molecular Weight
355.82
MDL Number
MFCD00672491
PubChem ID
16760350
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-L-aspartic acid b-benzyl ester chloromethylketone 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 therapeutic proteins and enzymes. Its protective groups help in controlling the reactivity of amino acids during synthesis.
  • Drug Development: It is used in the pharmaceutical industry for creating novel drug candidates. The chloromethylketone group can facilitate the formation of various bioactive compounds, enhancing the potential for new treatments.
  • Bioconjugation: Researchers employ this chemical in bioconjugation processes, where it aids in attaching biomolecules to surfaces or other molecules, improving drug delivery systems and diagnostic tools.
  • Research in Neuroscience: The compound is valuable in studies related to neurotransmitter pathways, particularly in understanding the role of aspartic acid derivatives in neuronal signaling.
  • Material Science: It finds applications in the development of polymers and materials that require specific functional groups for enhanced performance, such as in coatings or adhesives.

Citations