What unique challenges do researchers face in 4553-62-2

In some applications, this compound(4553-62-2)Computed Properties of C6H8N2 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 2-Methylglutaronitrile( cas:4553-62-2 ) is researched.Computed Properties of C6H8N2.Cooling, F. B.; Fager, S. K.; Fallon, R. D.; Folsom, P. W.; Gallagher, F. G.; Gavagan, J. E.; Hann, E. C.; Herkes, F. E.; Phillips, R. L.; Sigmund, A.; Wagner, L. W.; Wu, W.; DiCosimo, R. published the article 《Chemoenzymatic production of 1,5-dimethyl-2-piperidone》 about this compound( cas:4553-62-2 ) in Journal of Molecular Catalysis B: Enzymatic. Keywords: chemoenzymic dimethylpiperidone synthesis. Let’s learn more about this compound (cas:4553-62-2).

A chemoenzymic process for the preparation of 1,5-dimethyl-2-piperidone (1,5-DMPD) from 2-methylglutaronitrile (MGN) has been demonstrated. MGN was first hydrolyzed to 4-cyanopentanoic acid (4-CPA) ammonium salt using the nitrilase activity of immobilized Acidovorax facilis 72W cells. The hydrolysis reaction produced 4-CPA ammonium salt with greater than 98% regioselectivity at 100% conversion, and at concentrations of 170-210 g 4-CPA/l. Catalyst productivities of at least 1000 g 4-CPA/g dry cell weight (dcw) of immobilized cells were achieved by recycling the immobilized-cell catalyst in consecutive stirred-batch reactions. After recovery of the immobilized cell catalyst for reuse, the 4-CPA ammonium salt in the aqueous product mixture was directly converted to 1,5-DMPD by low-pressure catalytic hydrogenation in the presence of added methylamine.

In some applications, this compound(4553-62-2)Computed Properties of C6H8N2 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com