Ethyl 6-chloronicotinate
Ethyl 6-chloronicotinate
  • CAS No.:49608-01-7
Other grades of this product :
Ethyl 6-chloronicotinate Basic information
Product Name:Ethyl 6-chloronicotinate
Synonyms:3-Pyridinecarboxylic acid, 6-chloro-, ethyl ester;ETHYL 6-CHLORONICOTINATE[FOR TAZAROTENE];Ethyl 6-chloropyridine-3-carboxylate;ETHYL 2-CHLOROPYRIDINE-5-CARBOXYLATE;Ethyl 6-chloronicoti;2-Chloro-5-pyridinecarboxylicacid ethylester;Ethyl6-chloronicotinate,97%;Ethyl 2-chloropyridine-3-carboxylate, 6-Chloronicotinic acid ethyl ester
CAS:49608-01-7
MF:C8H8ClNO2
MW:185.61
EINECS:610-463-6
Product Categories:Building Blocks;C7 to C18;C8 to C9;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;Esters;Pyridines;Heterocycle-Pyridine series;carboxylic ester| alkyl chloride
Mol File:49608-01-7.mol
Ethyl 6-chloronicotinate Chemical Properties
Melting point 26-30 °C(lit.)
Boiling point 98 °C
density 1.245±0.06 g/cm3(Predicted)
refractive index 1.522
Fp >230 °F
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka-1.95±0.10(Predicted)
color Colourless to Off-White Oil to Low-Melting
BRN 4742175
InChIKeyILDJJTQWIZLGPO-UHFFFAOYSA-N
CAS DataBase Reference49608-01-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
Ethyl 6-chloronicotinate Usage And Synthesis
Chemical PropertiesWhite to light yellow solid or colorless to yellow liquid
UsesEthyl 6-chloronicotinate is a nicotinic acid derivative used in the preparation of potent H3 receptor antagonists.
UsesEthyl 6-chloropyridine-3-carboxylate (Ethyl 6-chloronicotinate) may be used in the preparation of ethyl 5-{[5-(1H-benzimidazol-2-yl)pyridin-2-yl]ethynyl}pyridine-2-carboxylate by reacting with 2-[6-(ethynyl)pyridin-3-yl]-1H-benzimidazole under microwave irradiation.
General DescriptionEthyl 6-chloropyridine-3-carboxylate (Ethyl-6-chloronicotinate, E-6-ClN) undergoes direct amidation on reacting with benzylamine in the presence lanthanum trifluoromethanesulfonate La(OTf)3. The structural and physicochemical properties of E-6-ClN have been investigated based on its spectroscopic data, time-dependent density functional theory and density of state diagrams.

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