CAS 1126-09-6: Ethyl isonipecotate

It is used as a reactant for synthesis of SMN protein modulators, β-aryl and β-amino-substituted aliphatic esters by rhodium catalyzed tandem double bond migration/conjugate addition, nitroethylenediamines by nucleophilic ring opening of nitroimidazolidinone. It is also involved in the reactions of RhoA inhibitors for cardiovascular disease therapy and saccharin derived Mannich bases as antimicrobials and antioxidants. It is employed as a reactant for one-pot reductive amination and Suzuki-Miyaura cross coupling of formyl aryl and heteroaryl MIDA boronates. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Ethyl piperidine-4-carboxylate

Ethyl Isonipecotate is an amine that is used as a chemical intermediate in the production of pharmaceuticals. It has been shown to inhibit the activity of histone deacetylases (HDACs) and may be useful for the treatment of inflammatory diseases. HDAC inhibitors, such as Ethyl Isonipecotate, inhibit the enzyme that removes acetyl groups from lysine residues on histones, preventing DNA condensation during transcriptional processes. This effect leads to increased transcription of genes involved in inflammation and immune response. Ethyl Isonipecotate has also been shown to have significant cytotoxicity against human cancer cells. The mechanism of action by which Ethyl Isonipecotate causes cytotoxicity is not known but may involve receptor binding or reaction with nitrogen nucleophiles.