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Catalog Number:
02294
CAS Number:
65853-65-8
N-2-Chlorobenzyloxycarbonyloxysuccinimide
Purity:
≥ 99% (HPLC)
Synonym(s):
Z(2-Cl)-OSu
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Product Information

N-2-Chlorobenzyloxycarbonyloxysuccinimide is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound serves as an effective protecting group for amines and alcohols, facilitating the selective modification of functional groups during complex chemical reactions. Its unique structure allows for enhanced stability and reactivity, making it an ideal choice for researchers looking to streamline their synthetic pathways.

In addition to its role in protecting group chemistry, N-2-Chlorobenzyloxycarbonyloxysuccinimide is also employed in the development of various bioactive molecules, including pharmaceuticals and agrochemicals. Its ability to selectively react under mild conditions provides significant advantages over traditional protecting groups, reducing the risk of side reactions and improving overall yields. Researchers and industry professionals can leverage this compound to enhance the efficiency of their synthetic processes, ultimately leading to faster development times and reduced costs in product formulation.

Synonyms
Z(2-Cl)-OSu
CAS Number
65853-65-8
Purity
≥ 99% (HPLC)
Molecular Formula
C12H10ClNO5
Molecular Weight
283.7
MDL Number
MFCD00010743
Melting Point
101-105º C
Appearance
White solid
Conditions
Store at RT
General Information
Synonyms
Z(2-Cl)-OSu
CAS Number
65853-65-8
Purity
≥ 99% (HPLC)
Molecular Formula
C12H10ClNO5
Molecular Weight
283.7
MDL Number
MFCD00010743
Melting Point
101-105º C
Appearance
White solid
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-2-Chlorobenzyloxycarbonyloxysuccinimide is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable reagent in the synthesis of peptides, facilitating the formation of peptide bonds with high efficiency, which is crucial for drug development and protein research.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Drug Delivery Systems: The compound is used in the development of advanced drug delivery systems, improving the targeting and release profiles of pharmaceuticals, which can lead to better patient outcomes.
  • Research in Cancer Therapy: Its application in cancer research helps in the design of targeted therapies, where it can be used to modify drugs for improved efficacy against specific cancer types.
  • Analytical Chemistry: This chemical is utilized in analytical methods for the detection and quantification of various compounds, aiding in quality control and regulatory compliance in pharmaceutical manufacturing.

Citations