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2,6-Dichloro-3-iodopyridine

Base Information
  • Chemical Name:2,6-Dichloro-3-iodopyridine
  • CAS No.:148493-37-2
  • Molecular Formula:C5H2Cl2IN
  • Molecular Weight:273.888
  • Hs Code.:2933399090
  • European Community (EC) Number:640-726-0
  • DSSTox Substance ID:DTXSID10371076
  • Nikkaji Number:J1.537.714C
  • Wikidata:Q72466568
  • Mol file:148493-37-2.mol
2,6-Dichloro-3-iodopyridine

Synonyms:2,6-Dichloro-3-iodopyridine;148493-37-2;Pyridine, 2,6-dichloro-3-iodo-;MFCD03094686;2,6-dichloro-3-iodo-pyridine;SCHEMBL1344323;DTXSID10371076;DPCQIHCGMIPSQV-UHFFFAOYSA-N;BCP22127;BBL101716;GEO-03682;STL555513;2,6-Dichloro-3-iodopyridine, 97%;2 pound not6-Dichloro-3-Iodopyridine;AKOS007930390;AC-9481;AM62365;CS-W010089;GS-6733;SY016472;A3253;D5061;FT-0643422;EN300-71557;W-205677

Suppliers and Price of 2,6-Dichloro-3-iodopyridine
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
  • TRC
  • 2,6-Dichloro-3-iodopyridine
  • 500mg
  • $ 60.00
  • TRC
  • 2,6-Dichloro-3-iodopyridine
  • 2.5g
  • $ 75.00
  • TCI Chemical
  • 2,6-Dichloro-3-iodopyridine >98.0%(GC)
  • 5g
  • $ 254.00
  • TCI Chemical
  • 2,6-Dichloro-3-iodopyridine >98.0%(GC)
  • 1g
  • $ 63.00
  • SynQuest Laboratories
  • 2,6-Dichloro-3-iodopyridine
  • 5 g
  • $ 31.00
  • SynQuest Laboratories
  • 2,6-Dichloro-3-iodopyridine
  • 1 g
  • $ 16.00
  • Sigma-Aldrich
  • 2,6-Dichloro-3-iodopyridine 97%
  • 1g
  • $ 77.00
  • Matrix Scientific
  • 2,6-Dichloro-3-iodopyridine 98%
  • 5g
  • $ 47.00
  • Matrix Scientific
  • 2,6-Dichloro-3-iodopyridine 98%
  • 100g
  • $ 235.00
  • Matrix Scientific
  • 2,6-Dichloro-3-iodopyridine 98%
  • 25g
  • $ 79.00
Total 91 raw suppliers
Chemical Property of 2,6-Dichloro-3-iodopyridine
Chemical Property:
  • Appearance/Colour:Light yellow powder 
  • Vapor Pressure:0.00279mmHg at 25°C 
  • Melting Point:74-79℃ 
  • Refractive Index:1.652 
  • Boiling Point:294.8 °C at 760 mmHg 
  • PKA:-3.87±0.10(Predicted) 
  • Flash Point:132.1 °C 
  • PSA:12.89000 
  • Density:2.129 g/cm3 
  • LogP:2.99300 
  • Storage Temp.:2-8°C 
  • Sensitive.:Light Sensitive 
  • Water Solubility.:Slightly soluble in water. 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:272.86090
  • Heavy Atom Count:9
  • Complexity:101
Purity/Quality:

99% *data from raw suppliers

2,6-Dichloro-3-iodopyridine *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi,Xn 
  • Statements: 22-37/38-41 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=NC(=C1I)Cl)Cl
  • Uses It is used as pharmaceutical raw material and intermediate.
Technology Process of 2,6-Dichloro-3-iodopyridine

There total 3 articles about 2,6-Dichloro-3-iodopyridine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
2,6-dichloropyridine; With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at -75 ℃; for 2h;
With iodine; In tetrahydrofuran;
DOI:10.1002/1099-0690(200104)2001:7<1371::AID-EJOC1371>3.0.CO;2-E
Guidance literature:
2,6-dichloropyridine; With n-butyllithium; In tetrahydrofuran; hexane; at -75 ℃; for 0.75h;
With iodine; In tetrahydrofuran; hexane; at -75 ℃; for 0.25h;
DOI:10.1021/jo047962z
Guidance literature:
2,6-dichloropyridine; With 2,2,6,6-tetramethyl-piperidine; n-butyllithium; ZnCl2-N,N,N’,N’-tetramethylethylenediamine; In tetrahydrofuran; at 20 ℃; for 2h; Inert atmosphere;
With iodine; In tetrahydrofuran; regioselective reaction; Inert atmosphere;
DOI:10.1002/chem.201101993
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