The important role of 10466-61-2

This compound(H-Leu-NH2.HCl)Application of 10466-61-2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Hydrolysis of hydrazide compounds by leucine aminopeptidase》. Authors are Wergin, A..The article about the compound:H-Leu-NH2.HClcas:10466-61-2,SMILESS:N[C@@H](CC(C)C)C(N)=O.[H]Cl).Application of 10466-61-2. Through the article, more information about this compound (cas:10466-61-2) is conveyed.

Hydrolysis of leucineamine-HCl (I), leucinehydrazide acetate (II), leucinehydrazinoacetamide acetate (III), and leucinesemicarbazide acetate (IV) by leucine aminopeptidase was optimum at pH 8-9. The spontaneous hydrolysis of the 3 hydrazides at pH 8.7 was relatively slow and could be neglected. The Km and activation energies E at 10-40° and pH 8.7 were [substrate, Km, (M), and E (kcal./mol) given]: I, 3.1 × 10-3, 10.5; II, 3.1 × 10-3, 10.5; III, 2.8 × 10-3, 9.8; IV, 0.72 × 10-3, 8.1.

This compound(H-Leu-NH2.HCl)Application of 10466-61-2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare