Ethyl 4-piperidinecarboxylate

Q: What is the Ethyl 4-piperidinecarboxylate?

Ethyl 4-piperidinecarboxylate is clear colorless to slightly brown liquid, while it's Molecular Formula is C8H15NO2. clear colorless to slightly brown liquid It is used as a reactant for synthesis of SMN protein modulators, ß-aryl and ß-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.

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1.What is the Ethyl 4-piperidinecarboxylate ?

clear colorless to slightly brown liquid

Ethyl 4-piperidinecarboxylate is a versatile chemical compound with a clear colorless to slightly brown liquid appearance. It serves as a key reactant in the synthesis of various organic compounds and has applications in different industries due to its unique chemical properties.

2.What is the CAS number for Ethyl 4-piperidinecarboxylate ?

The CAS number of Ethyl 4-piperidinecarboxylate is 1126-09-6.

3.What are another words for Ethyl 4-piperidinecarboxylate ?

Synonyms?for?Ethyl 4-piperidinecarboxylate 1126-09-6:ethyl piperidine-4-carboxylate;Isonipecoticacid, ethyl ester (6CI,7CI,8CI);4-(Ethoxycarbonyl)piperidine;4-Carboethoxypiperidine;Ethyl 4-piperidinecarboxylate;

4.What is Ethyl 4-piperidinecarboxylate (1126-09-6) used for?

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.

InChI:InChI=1/C8H15NO2/c1-2-11-8(10)7-3-5-9-6-4-7/h7,9H,2-6H2,1H3/p+1

Relevant articles related to Ethyl 4-piperidinecarboxylate:

Article	Source
Synthesis and SAR studies of 1-substituted-n-(4-alkoxycarbonylpiperidin-1-yl)alkanes as potent antiarrhythmic agents	Tripathi, Ravish C.,Pandey, Suresh K.,Kar,Dikshit,Saxena, Anil K. , p. 2693 - 2698 (1999)
A novel approach for the synthesis of hydrogel nanoparticles and a removal study of reactive dyes from industrial effluent	Mahida, Viran P.,Patel, Manish P. , p. 21577 - 21589 (2016)
Late-Stage Intermolecular Allylic C-H Amination	Clark, Joseph R.,Dixon, Charlie F.,Feng, Kaibo,Han, Wei,Ide, Takafumi,Koch, Vanessa,Teng, Dawei,Wendell, Chloe I.,White, M. Christina supporting information, p. 14969 - 14975 (2021/10/01)

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