Synthetic Route of 139290-70-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.139290-70-3, Name is tert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate, molecular formula is C13H24N2O4. In a article，once mentioned of 139290-70-3
Heterocyclic compounds of structural formula (I), or a pharmaceutically acceptable salt thereof, wherein W is a R 1 -substituted heteroaryl, R 1 is an heteroaryl ring substituted with an ester or carboxylic acid containing radical, X-T is N-CR 5 R 6 , C=CR 5 or CR 13 -CR 5 R 6 , Y is a bond or -C(O)-, a and b represent an integer selected from 1 to 4, and Ar is an optionally substituted phenyl or naphtyl, are inhibitors of stearoyl-coenzyme A delta-9 desaturase (SCD) The heterocyclic compounds are useful for the prevention and treatment of conditions related to abnormal lipid synthesis and metabolism, including cardiovascular disease, atherosclerosis, obesity, diabetes, neurological disease, Metabolic Syndrome, insulin resistance, cancer, liver steatosis, and non-alcoholic steatohepatitis.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 139290-70-3, and how the biochemistry of the body works.Synthetic Route of 139290-70-3
Reference：
Piperidine – Wikipedia,
Piperidine | C5H22085N – PubChem