ChemicalBook Product Catalog Chemical Reagents Organic reagents Esters Ethyl compound Ethyl 1-methylnipecotate

Ethyl 1-methylnipecotate

Ethyl 1-methylnipecotate Basic information
Product Name:Ethyl 1-methylnipecotate
Synonyms:Ethyl 1-methylnipecotate, 98+%;1-Methyl-3-piperidinecarboxylic acid ethyl ester;ETHYL 1-METHYLPIPERIDINE-3-CARBOXYLATE;ETHYL 1-METHYLNIPECOTATE;ETHYL 1-METHYL-3-PIPERIDINE-CARBOXYLATE;Ethyl 1-methylpiperidine-3-carboxylate 97%;Ethyl N-Methyl piperidine-3-carboxylate or Ethyl 1-Methylnipecotate;Ethyl N-Methylpiperidine-3-carboxylate
CAS:5166-67-6
MF:C9H17NO2
MW:171.24
EINECS:225-951-0
Product Categories:Heterocyclic Compounds
Mol File:5166-67-6.mol
Ethyl 1-methylnipecotate Structure
Ethyl 1-methylnipecotate Chemical Properties
Boiling point 88-89 °C/11 mmHg (lit.)
density 0.954 g/mL at 25 °C (lit.)
refractive index n20/D 1.451(lit.)
Fp 155 °F
storage temp. Sealed in dry,Room Temperature
pka8.56±0.10(Predicted)
form clear liquid
color Colorless to Almost colorless
BRN 123259
CAS DataBase Reference5166-67-6(CAS DataBase Reference)
NIST Chemistry ReferenceEthyl 1-methylnipecotate(5166-67-6)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39-37/39
WGK Germany 3
F 9-23
Hazard Note Irritant
HS Code 29333990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
Ethyl 1-methylnipecotate Usage And Synthesis
Chemical PropertiesClear colorless to pale yellow liquid
UsesReactant for:
N-demethylation of tertiary amines
Reverse cope elimination reactions
Regioselective oxidation
Synthesis of chelating agents
Sequential Michael-Michael-Dieckmann cyclizations
General DescriptionEnantiomeric discrimination has been investigated in 1H and 13C NMR spectra of ethyl 1-methyl-3-piperidinecarboxylate in the presence of (-)-(18-crown-6)-2,3,11,12-tetracarboxylic acid.
Ethyl 1-methylnipecotate Preparation Products And Raw materials
Preparation Products3-Piperidinemethanol,1-methyl-,(3R)-(9CI)
Methyl 4-Methylisonipecotic acid ethyl ester Ethyl (2R,4R)-1-(Nitroglycerine-nitro-L-arginyl)-4-methyl-piperidinecarboxylate hydrochloride 1-Boc-4-(Cyanomethyl)-4-Piperidine carboxylic Acid Ethyl Ester Ethyl 3-methylpiperidine-3-carboxylate N-Cbz-3-Methylnipecotic acid ethyl ester Ethyl 1-Boc-3-methylpiperidine-3-carboxylate Ethyl 1-methylpipecolinate Ethyl (2R,4R)-4-methyl-2-piperidinecarboxylate Ethyl N-Boc-4-methylpiperidine-4-carboxylate 2-PIPERIDINECARBOXYLIC ACID, 1-[5-[IMINO(NITROAMINO)METHYL]AMINO]-2-[[(3-METHYL-8-QUINOLINYL)SULFONYL]AMINO]-1-OXOPENTYL]-4-METHYL-,ETHYL ESTER,[2R-[1(S*), 2ALPHA, 4BETA]]- Ethyl 4-piperidinecarboxylate N-Cbz-4-Methylisonipecotic acid ethyl ester Ethyl 4-Methylpiperidine-4-carboxylate Hydrochloride 1-ethoxycarbonylmethyl-piperidine-2-carboxylic acidethyleste 1-Boc-3-(Cyanomethyl)-3-Piperidine carboxylic Acid Ethyl Ester N-Boc-3-Methylnipecotic acid ethyl ester METHYL THIOPHENE-2-CARBOXYLATE
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