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2,3-Dichloropyridine

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2,3-Dichloropyridine Basic information

Product Name:
2,3-Dichloropyridine
Synonyms:
  • 2,3-dichloro-pyridin
  • 2,3-dichloropyridine analogue
  • 2,3-DICHLOROPYRIDINE
  • 2,3-Dichloropyridine147.99
  • 2,3-Dichloropyridine,99%
  • 2,3-DICHLOROPYRIDINE 2,3-DICHLOROPYRIDINE
  • 2,3-dichloropydine
  • 2,3-Dichloropyridine ,98%
CAS:
2402-77-9
MF:
C5H3Cl2N
MW:
147.99
EINECS:
219-281-8
Product Categories:
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Pyridine series
  • Chloropyridines
  • Halopyridines
  • Boronic Acid
  • C5Heterocyclic Building Blocks
  • blocks
  • Pyridines
  • Pyridine
  • Halides
  • Heterocycles
  • Pyridines derivates
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Chlorinated heterocyclic series
  • alkyl chloride
  • bc0001
Mol File:
2402-77-9.mol
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2,3-Dichloropyridine Chemical Properties

Melting point:
64-67 °C (lit.)
Boiling point:
242.42°C (rough estimate)
Density 
1.5159 (rough estimate)
refractive index 
1.5500 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
form 
Crystalline Powder
pka
-0.63±0.10(Predicted)
color 
White to slightly beige
Water Solubility 
slightly soluble
BRN 
109811
InChI
InChI=1S/C5H3Cl2N/c6-4-2-1-3-8-5(4)7/h1-3H
InChIKey
MAKFMOSBBNKPMS-UHFFFAOYSA-N
SMILES
C1(Cl)=NC=CC=C1Cl
CAS DataBase Reference
2402-77-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36-37/39
RIDADR 
UN2811
WGK Germany 
3
RTECS 
US8050000
Hazard Note 
Irritant
HazardClass 
6.1
HS Code 
29333999

MSDS

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2,3-Dichloropyridine Usage And Synthesis

Chemical Properties

White to slightly beige crystalline powder

Uses

2,3-Dichloropyridine is used as a reagent for the preparation of substituted 3-(5-membered heterocycle-carboxamido)pyridine derivatives for treatment of autoimmune and inflammatory diseases. Also in the synthesis, crystal structure and biological activity of novel anthranilic Diamide insecticide with propargyl ether.

Synthesis

2,3-dichloropyridine is synthesized from 2-chloronicotinic acid via amidation, Hofmann degradation, diazotization and Sandmeyer reaction.

2,3-Dichloropyridine Preparation Products And Raw materials

Preparation Products

2,3-DichloropyridineSupplier

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