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Ethyl 6-chloronicotinate

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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
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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
Flash point:
>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
BRN 
4742175
InChIKey
ILDJJTQWIZLGPO-UHFFFAOYSA-N
CAS DataBase Reference
49608-01-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900

MSDS

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Ethyl 6-chloronicotinate Usage And Synthesis

Chemical Properties

White to light yellow solid or colorless to yellow liquid

Uses

Ethyl 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.

Uses

Ethyl 6-chloronicotinate is a nicotinic acid derivative used in the preparation of potent H3 receptor antagonists.

General Description

Ethyl 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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