CAS 201489-21-6
:N-(9-fluorenylmethoxycarbonyl)-L-alanine-3-13C
Description:
N-(9-fluorenylmethoxycarbonyl)-L-alanine-3-13C, identified by its CAS number 201489-21-6, is a derivative of the amino acid L-alanine, which is modified to include a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is characterized by its stable structure, which is essential for use in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The incorporation of the 13C isotope at the third carbon position of the alanine side chain allows for applications in NMR spectroscopy and metabolic studies, providing insights into metabolic pathways and protein dynamics. The Fmoc group is commonly used in organic synthesis due to its ease of removal under mild basic conditions, making it a popular choice for protecting amino groups during peptide synthesis. Overall, this compound serves as a valuable tool in biochemistry and molecular biology, facilitating the study of protein structure and function.
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Found 3 products.
Fmoc-Ala-OH-3-13C
CAS:<p>Fmoc-Ala-OH-3-13C is a versatile building block that can be used to synthesize a variety of compounds. It is an intermediate in the synthesis of more complex compounds and has been shown to possess high reactivity in peptide coupling reactions. Fmoc-Ala-OH-3-13C has a CAS number of 201489-21-6 and is a fine chemical that can be used for research, development, and other purposes.</p>Formula:CC17H17NO4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:312.32 g/mol
