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N-[(9H-fluoren-9-ylmethoxy)carbonyl] CAS:29022-11-5

N-[(9H-fluoren-9-ylmethoxy)carbonyl] is a chemical moiety commonly utilized in peptide synthesis and organic chemistry. This functional group serves as a critical component for the protection of amino acids during peptide bond formation, playing a pivotal role in the controlled assembly of complex peptides and peptidomimetics.

 


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Application and Effect:

The N-[(9H-fluoren-9-ylmethoxy)carbonyl] moiety holds significant importance in peptide synthesis, where it acts as a protective group for the amino acids' reactive functional groups. By incorporating this moiety, researchers can selectively shield specific reactive sites of amino acids, ensuring precise amide bond formation during peptide elongation. This controlled protection enables the synthesis of high-purity peptide sequences with tailored functionalities, essential for investigating biological activities and developing novel therapeutic agents. Moreover, N-[(9H-fluoren-9-ylmethoxy)carbonyl] finds extensive application in the creation of peptide-based pharmaceuticals, biochemical probes, and biomaterials. Through the strategic incorporation of this moiety into peptide structures, scientists can modulate the properties of the resulting molecules to exhibit targeted biological activities, such as receptor binding, enzyme inhibition, or cellular uptake. This versatility makes the compound invaluable in drug development, structural biology, and biotechnological advancements. Furthermore, the precise chemical characteristics of N-[(9H-fluoren-9-ylmethoxy)carbonyl] contribute to its utility in producing peptide conjugates for targeted drug delivery and as molecular tools for studying protein-protein interactions. Its applications extend to various scientific disciplines, including medicinal chemistry, bioengineering, and pharmacology, emphasizing its vital role in advancing research and enabling the development of innovative medical solutions. In summary, N-[(9H-fluoren-9-ylmethoxy)carbonyl] serves as a fundamental building block in peptide chemistry, facilitating the construction of diverse peptide structures with tailored functionalities. Its broad range of applications spans across drug development, biochemical research, and biotechnology, underscoring its significance in advancing scientific knowledge and contributing to the development of novel therapeutic interventions.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C17H15NO4
Assay 99%
Appearance white powder
CAS No.  29022-11-5
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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