Some scientific research about 10466-61-2

《Enzymic synthesis of peptide in acetonitrile/supercritical carbon dioxide》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(H-Leu-NH2.HCl)Synthetic Route of C6H15ClN2O.

Synthetic Route of C6H15ClN2O. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: H-Leu-NH2.HCl, is researched, Molecular C6H15ClN2O, CAS is 10466-61-2, about Enzymic synthesis of peptide in acetonitrile/supercritical carbon dioxide. Author is Noritomi, Hidetaka; Miyata, Motokazu; Kato, Satoru; Nagahama, Kunio.

The peptide synthesis from Ac-Tyr-OEt and amino acid amides was realized using α-chymotrypsin in MeCN or acetonitrile/supercritical carbon dioxide (SC-CO2) containing small amounts of water. In both solvent systems there was an optimum water content for peptide synthesis, above which peptide hydrolysis became more important. After an incubation for 5 h, the yields of the peptide was 64% in MeCN and 91% in MeCN/SC-CO2, resp.

《Enzymic synthesis of peptide in acetonitrile/supercritical carbon dioxide》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(H-Leu-NH2.HCl)Synthetic Route of C6H15ClN2O.

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare