CasNo.1126-09-6,Ethyl 4-piperidinecarboxylate,(1126-09-6) Suppliers

1 Gram	Negotiable

Min.Order :1 Gram
Purity: 98%
Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

Ethyl 4-piperidinecarboxylate 1126-09-6 high purity Ethyl 4-piperidinecarboxylate

Quick Details

Appearance:Clear colorless to slightly brown Liquid
Application:intermediate
PackAge:drum
ProductionCapacity:1|Kilogram|Month
Storage:Keep in dark place,Inert atmosphere,Room temperature
Transportation:According to your request

Superiority:

Product Name:	Ethyl 4-piperidinecarboxylate
Synonyms:	4-Carbethoxypiperidine;ISONIPECOTINIC ACID ETHYL ESTER;Ethyl isonipecotate ,97%;1-ethylpiperidine-4-carboxylate;ethyl piperidin-4-carboxylate;Ethyl isonipecotate, 98+% 100GR;Ethyl isonipecotate, 98+% 25GR;Ethyl Isonipecotate Isonipecotic Acid Ethyl Ester 4-Piperidinecarboxylic Acid Ethyl Ester
CAS:	1126-09-6
MF:	C8H15NO2
MW:	157.21
EINECS:	214-416-7
Product Categories:	Heterocycles;Building Blocks;C8;Chemical Synthesis;Heterocyclic Building Blocks;Piperidines;Pharmaceutical Intermediates;Piperidines, Piperidones, Piperazines;pharmacetical;AMINOACIDS DERIVATIVES;Piperidine;Intermediate;john's
Mol File:	1126-09-6.mol
Uses	Reactant for synthesis of:• ;SMN protein modulators1• ;β-aryl and β-amino-substituted aliphatic esters by rhodium catalyzed tandem double bond migration/conjugate addition2• ;Nitroethylenediamines by nucleophilic ring opening of nitroimidazolidinone3• ;RhoA inhibitors for cardiovascular disease therapy4• ;Saccharin derived Mannich bases as antimicrobials and antioxidants5Reactant for one-pot reductive amination and Suzuki-Miyaura cross coupling of formyl aryl and heteroaryl MIDA boronates6
Uses	Reactant for synthesis of SMN protein modulators and β-aryl and β-amino-substituted aliphatic esters by rhodium catalyzed tandem double bond migration/conjugate addition.
Uses	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.

Details:

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We can provide customers with small quantities with gram level for laboratories research to tonnage level for industrial production Synthesis capacity from 1 liter to 5000 liter is available.