Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Cyanopyridine >  2-Cyano-3-chloropyridine

2-Cyano-3-chloropyridine

Basic information Safety Supplier Related

2-Cyano-3-chloropyridine Basic information

Product Name:
2-Cyano-3-chloropyridine
Synonyms:
  • 2-Cyano-3-chloropyri
  • 3-Chloropicolinonitrile
  • 3-Chloro-2-cyanopyridine ,95%
  • 3-Chloro-2-cyanopyridine, 3-Chloropicolinonitrile
  • 3-CHLORO-2-PYRIDINECARBONITRILE
  • 3-CHLORO-2-CYANOPYRIDINE
  • 3-CHLOROPYRIDINE-2-CARBONITRILE
  • 2-CYANO-3-CHLORO PYRIDINE / 3-CHLORO-2-CYANOPYRIDINE
CAS:
38180-46-0
MF:
C6H3ClN2
MW:
138.55
EINECS:
641-299-3
Product Categories:
  • Heterocycle-Pyridine series
  • Nucleotides and Nucleosides
  • Pyridines
  • Bases & Related Reagents
  • Pyridines, Pyrimidines, Purines and Pteredines
  • pharmacetical
  • Pyridine series
  • Pyridine
  • Nucleotides
Mol File:
38180-46-0.mol
More
Less

2-Cyano-3-chloropyridine Chemical Properties

Melting point:
81-83°C
Boiling point:
100°C/3mmHg(lit.)
Density 
1.33±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Methanol
pka
-2.60±0.10(Predicted)
form 
Solid
color 
Light Yellow
InChI
InChI=1S/C6H3ClN2/c7-5-2-1-3-9-6(5)4-8/h1-3H
InChIKey
YDPLFBIGFQFIDB-UHFFFAOYSA-N
SMILES
C1(C#N)=NC=CC=C1Cl
CAS DataBase Reference
38180-46-0(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
T,Xi
Risk Statements 
25-36/37/38-20/21/22
Safety Statements 
45-36/37-22
RIDADR 
2811
HazardClass 
6.1
HazardClass 
IRRITANT-HARMFUL
PackingGroup 
HS Code 
29333990
More
Less

2-Cyano-3-chloropyridine Usage And Synthesis

Chemical Properties

Light Yellow Solid

Uses

2-Cyano-3-chloropyridine (cas# 38180-46-0) is a compound useful in organic synthesis.

Synthesis

7677-24-9

38180-46-0

3-Chloro-2-cyanopyridine (44A, 2.59 g, 20 mmol) was used as starting material and mixed with trimethylmethylsilyl cyanide (5.95 g, 60 mmol), triethylamine (Et3N, 4.05 g, 40 mmol), and acetonitrile (20 mL) in a 250 mL three-necked round-bottom flask. The reaction mixture was refluxed under nitrogen protection for 6 h. Complete consumption of raw materials was confirmed by HPLC analysis. Upon completion of the reaction, the cooled reaction mixture was concentrated under reduced pressure to give a brown semi-solid. The semi-solid was extracted by partitioning with 3N Na2CO3 aqueous solution and dichloromethane (CH2Cl2). The organic layer was washed sequentially with water and brine, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was purified by fast chromatography using 5% ether (Et2O)/dichloromethane (CH2Cl2) as eluent, and the target product 44B was finally obtained as a white crystalline solid (1.84 g, 67% yield). The structure of the product was confirmed by 1H NMR (CDCl3): δ 7.37 (dd, J = 4.7, 8.4 Hz, 1H), 7.73 (dd, J = 1.4, 8.2 Hz, 1H), 8.47 (dd, J = 1.3, 4.6 Hz, 1H); LC/MS analysis showed m/z 139 [M + H]+.

References

[1] Patent: US2004/19063, 2004, A1
[2] Patent: US2004/181064, 2004, A1

2-Cyano-3-chloropyridine Preparation Products And Raw materials

Raw materials

2-Cyano-3-chloropyridineSupplier

Jinan LuoHe PharmaTech Co., Ltd. Gold
Tel
86-0531-68658065 15726150375
Email
1071018499@qq.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-021-61259138 18621169109
Email
market03@meryer.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com