The effect of the change of synthetic route on the product 3235-67-4

Here is just a brief introduction to this compound(3235-67-4)Product Details of 3235-67-4, more information about the compound(1-Piperidineacetic Acid) is in the article, you can click the link below.

Product Details of 3235-67-4. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 1-Piperidineacetic Acid, is researched, Molecular C7H13NO2, CAS is 3235-67-4, about On the cleavage of N-C linkage of piperidine N-derivatives by mouse and rat liver enzyme system. Author is Kimura, Katsuhiko; Nagaoka, Masao; Nakazawa, Shuichi; Ohgiya, Shozaburo.

The cleavage of the N-C bond of piperidine derivatives by the 9000 × g supernatant of rat liver was more readily carried out than that by the supernatant of mouse liver. The cleavage of N-Et derivatives such as N-methylpiperidine (I) [626-67-5] and N-ethylpiperidine [766-09-6] was not readily carried out by these supernatants, whereas that of the Mannich bases was done readily. The addition of phenobarbital accelerated N-C bond cleavage, but 3-methylcholanthrene was without effect. Pretreatment of the animals with SKF-525A inhibited the cleavage.

Here is just a brief introduction to this compound(3235-67-4)Product Details of 3235-67-4, more information about the compound(1-Piperidineacetic Acid) is in the article, you can click the link below.

Reference:
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem