Application of 236406-39-6, In heterogeneous catalysis, the catalyst is in a different phase from the reactants. At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 236406-39-6, name is 8-Boc-2,8-Diazaspiro[4.5]decane. In an article，Which mentioned a new discovery about 236406-39-6
The synthesis of nine new 2-methyl-10-propargylquinazoline antifolates with substituents in the p-aminobenzoyl ring is described. In general the synthetic route involved the coupling of the appropriate ring-substituted diethyl N-[4-(prop-2-ynylamino)benzoyl]-L-glutamate with 6-(bromomethyl)-3,4-dihydro-2-methyl-4-oxoquinazoline (11) followed by deprotection using mild alkali. The compounds were tested as inhibitors of partially purified L1210 thymidylate synthase (TS). They were also examined for their inhibition of the growth L1210 cells in culture. Compared to the parent compound 1a the 2′-fluoro analogue 2a exhibited enhanced potency in both systems whereas the 3′-fluoro analogue 3a showed enhanced growth inhibitory properties against L1210 cells despite being a poorer inhibitor of the isolated enzyme. Chloro, hydroxy, methoxy, and nitro substituents in the 2′-position were also well tolerated by the enzyme but failed to give enhanced growth inhibition. The series was extended to cover analogues of the 2′-fluoro, 3′-fluoro, 2′-chloro, 2′-methyl, 2′-amino, 2′-methoxy, and 2′-nitro derivatives with modified alkyl substituents at N10.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.236406-39-6. In my other articles, you can also check out more blogs about 236406-39-6
Reference：
Piperidine – Wikipedia,
Piperidine | C5H19353N – PubChem