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

1 Kilogram	Negotiable

Min.Order :1 Kilogram
Purity: 98.0% Min
Payment Terms : L/C,T/T,

Keywords

1126-09-6 Ethyl 4-piperidinecarboxylate C8H15NO2

Quick Details

Appearance:conform
Application:For Organic synthsis
PackAge:As per customer's
ProductionCapacity:1|Metric Ton|Day
Storage:Room temperature
Transportation:To be shipped as non-hazardous chemicals

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Details:

Ethyl 4-piperidinecarboxylate Basic information

Product Name:	Ethyl 4-piperidinecarboxylate
Synonyms:	4-Carbethoxypiperidine;ISONIPECOTINIC ACID ETHYL ESTER;ISONIPECOTIC ACID ETHYL ESTER;ETHYL ISONIPECOTATE;ETHYL PIPERIDINE-4-CARBOXYLATE;ETHYL 4-PIPERIDINECARBOXYLATE;LABOTEST-BB LT00159543;4-PIPERDINECARBOXYLIC ACID, ETHYL ESTER
CAS:	1126-09-6
MF:	C8H15NO2
MW:	157.21
EINECS:	214-416-7
Product Categories:	Pharmaceutical Intermediates;Piperidines, Piperidones, Piperazines;pharmacetical;AMINOACIDS DERIVATIVES;Piperidine;Building Blocks;C8;Chemical Synthesis;Heterocyclic Building Blocks;Piperidines;Heterocycles
Mol File:	1126-09-6.mol

Ethyl 4-piperidinecarboxylate Chemical Properties

bp	204 °C(lit.)
density	1.02 g/mL at 25 °C(lit.)
refractive index	n20/D 1.459(lit.)
Fp	176 °F
Water Solubility	miscible
BRN	118419
CAS DataBase Reference	1126-09-6(CAS DataBase Reference)
NIST Chemistry Reference	Ethyl piperidine-4-carboxylate(1126-09-6)

Safety Information

Hazard Codes	C,Xi
Risk Statements	34-36/37/38
Safety Statements	23-24/25-36-26
WGK Germany	3
Hazard Note	Irritant
HS Code	29333999

MSDS Information

Provider	Language
Ethyl 4-piperidinecarboxylate	English
SigmaAldrich	English
ACROS	English
ALFA	English

Ethyl 4-piperidinecarboxylate Usage And Synthesis

Chemical Properties	clear colorless to slightly brown liquid
Usage	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
Usage	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.