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Technology Process of 2-Chloronicotinic acid hydrochloride

2-Chloronicotinic acid hydrochloride

Base Information
  • Chemical Name:2-Chloronicotinic acid hydrochloride
  • CAS No.:56055-55-1
  • Molecular Formula:C6H5Cl2NO2
  • Molecular Weight:194.017
  • Hs Code.:2933399090
  • DSSTox Substance ID:DTXSID30376462
  • Mol file:56055-55-1.mol
2-Chloronicotinic acid hydrochloride

Synonyms:2-Chloronicotinic acid hydrochloride;56055-55-1;2-chloropyridine-3-carboxylic Acid Hydrochloride;2-chloro-3-pyridinecarboxylic acid hydrochloride;2-chloropyridine-3-carboxylic acid;hydrochloride;2-Chloronicotinicacid hydrochloride;ACIDBLUE40;2-chloropyridine-3-carboxylic acid,hydrochloride;SCHEMBL587011;chloronicotinic acid hydrochloride;DTXSID30376462;HGILEOFUZXHTHB-UHFFFAOYSA-N;AKOS015891644;2-chloropyridin-3-carboxylic acid HCl salt;FT-0646330;A830905;2-chloranylpyridine-3-carboxylic acid hydrochloride;2-Chloropyridine-3-carboxylic acid--hydrogen chloride (1/1)

Suppliers and Price of 2-Chloronicotinic acid hydrochloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 2-CHLOROPYRIDINE-3-CARBOXYLIC ACID HYDROCHLORIDE 95.00%
  • 5G
  • $ 909.56
Total 14 raw suppliers
Chemical Property of 2-Chloronicotinic acid hydrochloride
Chemical Property:
  • Vapor Pressure:0.000168mmHg at 25°C 
  • Boiling Point:316.8 °C at 760 mmHg 
  • Flash Point:145.4 °C 
  • PSA：50.19000 
  • LogP:2.23520 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:192.9697338
  • Heavy Atom Count:11
  • Complexity:140
Purity/Quality:

99% *data from raw suppliers

2-CHLOROPYRIDINE-3-CARBOXYLIC ACID HYDROCHLORIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=C(N=C1)Cl)C(=O)O.Cl
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