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4-CHLORO-PYRIDINE-2-CARBONITRILE

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4-CHLORO-PYRIDINE-2-CARBONITRILE Basic information

Product Name:
4-CHLORO-PYRIDINE-2-CARBONITRILE
Synonyms:
  • 2-Cyano-4-chloropyridine, 4-Chloro-2-cyanopyridine, 4-Chloropicolinonitrile
  • 4-Chloro-2-pyridinecarbonitrile
  • 1-chloropicolinonitrile
  • 4-Chloro-2-cyanopyridine, 4-Chloropicolinonitrile
  • 4-Chloro-2-pyridinecarbonitrile 97%
  • IFLAB-BB F3099-7226
  • 4-CHLORO-2-CYANOPYRIDINE
  • 4-CHLOROPICOLINONITRILE
CAS:
19235-89-3
MF:
C6H3ClN2
MW:
138.55
EINECS:
606-272-2
Product Categories:
  • Pyridine series
  • blocks
  • Carboxes
  • Pyridines
  • Boron, Nitrile, Thio,& TM-Cpds
  • Heterocycles
Mol File:
19235-89-3.mol
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4-CHLORO-PYRIDINE-2-CARBONITRILE Chemical Properties

Melting point:
81-85 °C
Boiling point:
231.6±20.0 °C(Predicted)
Density 
1.33±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
-2.74±0.10(Predicted)
color 
White to Yellow to Orange
InChI
InChI=1S/C6H3ClN2/c7-5-1-2-9-6(3-5)4-8/h1-3H
InChIKey
DYEZRXLVZMZHQT-UHFFFAOYSA-N
SMILES
C1(C#N)=NC=CC(Cl)=C1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-41
Safety Statements 
26-39
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
HazardClass 
IRRITANT
PackingGroup 
III
HS Code 
29333990
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4-CHLORO-PYRIDINE-2-CARBONITRILE Usage And Synthesis

Chemical Properties

Type of white solid

Uses

Substrate used to prepare chiral dialkylaminopyridines bearing a C-2 hydroxyalkyl group via biocatalysis.

Synthesis

1121-76-2

7677-24-9

19235-89-3

4-Chloropyridine N-oxide (7.53 g, 58.1 mmol) and N,N-dimethylcarbamoyl chloride (9.36 g, 87.0 mmol) were mixed in acetonitrile (200 mL). Subsequently, trimethylcyanosilane (11.5 g, 116 mmol) was added slowly and dropwise to the reaction system. The reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, the mixture was combined with ethyl acetate and water for extraction. The organic layer was washed sequentially with saturated aqueous sodium bicarbonate and saturated saline, and then dried with magnesium sulfate. The solvent was removed by distillation and the residue obtained was purified by column chromatography (silica gel 200 g) using hexane-ethyl acetate (3:1, v/v) as eluent. The target fraction was collected and concentrated to give 4-chloro-2-cyanopyridine (8.05 g, 99% yield) as a light yellow oil. The product was characterized by 1H-NMR (CDCl3) and IR (KBr): 1H-NMR δ 7.54-7.56 (1H, m), 7.72 (1H, s), 8.63 (1H, d, J = 5.3 Hz); IR 2239, 1568, 1549, 1462, 1379, 1288, 1215, 844, 704 cm-1.

References

[1] Patent: EP1424336, 2004, A1. Location in patent: Page 219
[2] Patent: US2006/160803, 2006, A1. Location in patent: Page/Page column 146
[3] Tetrahedron Asymmetry, 2005, vol. 16, # 20, p. 3427 - 3435
[4] Patent: WO2005/95326, 2005, A2. Location in patent: Page/Page column 225-226
[5] Patent: WO2005/87215, 2005, A1. Location in patent: Page/Page column 143

4-CHLORO-PYRIDINE-2-CARBONITRILE Preparation Products And Raw materials

Raw materials

4-CHLORO-PYRIDINE-2-CARBONITRILESupplier

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