Ethyl 4-piperidinec...

Ethyl 4-piperidinecarboxylate

Ethyl 4-piperidinecarboxylate

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1 Kilogram

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  • 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 Structure
 
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.

 

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