N-(9-Fluorenylmethoxycarbonyl)-L-proline pentafluorophenyl ester is a chemical compound commonly used in peptide synthesis and related applications. It features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The presence of the pentafluorophenyl ester moiety enhances the reactivity of the carboxylic acid, facilitating the formation of peptide bonds. This compound is characterized by its relatively high molecular weight and specific functional groups that contribute to its solubility and reactivity. It is typically handled under controlled conditions due to its potential reactivity and the need for careful management of the protecting groups during synthesis. The compound's structure allows for selective reactions, making it a valuable intermediate in the synthesis of complex peptides and other bioactive molecules. As with many chemical substances, safety precautions should be observed when handling this compound, including the use of appropriate personal protective equipment.

N-(9-FLUORENYLMETHOXYCARBONYL)-L-PROLINE PENTAFLUOROPHENYL ESTER

125281-38-1: N-(9-Fluorenylmethoxycarbonyl)-L-proline pentafluorophenyl ester is a chemical compound commonly used in peptide synthesis and related applications. It features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The presence of the pentafluorophenyl ester moiety enhances the reactivity of the carboxylic acid, facilitating the formation of peptide bonds. This compound is characterized by its relatively high molecular weight and specific functional groups that contribute to its solubility and reactivity. It is typically handled under controlled conditions due to its potential reactivity and the need for careful management of the protecting groups during synthesis. The compound's structure allows for selective reactions, making it a valuable intermediate in the synthesis of complex peptides and other bioactive molecules. As with many chemical substances, safety precautions should be observed when handling this compound, including the use of appropriate personal protective equipment.

CAS 125281-38-1

N-(9-FLUORENYLMETHOXYCARBONYL)-L-PROLINE PENTAFLUOROPHENYL ESTER

Fmoc-D-Pro-OPfp

Ref: IN-DA000NFI

Fmoc-D-Pro-OPfp

Ref: 54-PC48018