Recommanded Product: 51644-96-3In 2017 ,《Solvent-free mechanochemical deprotection of N-Boc group》 was published in International Journal of Organic Chemistry. The article was written by Djud, Mateja; Margetic, Davor. The article contains the following contents:
Boc protection group could be readily removed in a very mild mechanochem. conditions. In a short reaction time, ball milling of Boc-protected amines with p-toluenesulfonic acid in solvent-free conditions affords corresponding amine p-TsOH salts. In addition to this study using tert-Butyl (5-aminopentyl)carbamate, there are many other studies that have used tert-Butyl (5-aminopentyl)carbamate(cas: 51644-96-3Recommanded Product: 51644-96-3) was used in this study.
Some of the reported applications of tert-Butyl (5-aminopentyl)carbamate(cas: 51644-96-3) include: synthesis of of a supermacrocycle that self-assemble to form organic nanotubes., preparation of water-soluble unsymmetrical sulforhodamine fluorophores from monobrominated sulfoxanthene dye, synthesis of functionalized porphyrins as biocompatible carrier system for photodynamic therapy (PDT).Recommanded Product: 51644-96-3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics