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Ethyl 3-(chloromethyl)isonicotinate

Base Information Edit
  • Chemical Name:Ethyl 3-(chloromethyl)isonicotinate
  • CAS No.:58553-54-1
  • Molecular Formula:C9H10ClNO2
  • Molecular Weight:199.637
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50482493
  • Wikidata:Q82318869
  • Mol file:58553-54-1.mol
Ethyl 3-(chloromethyl)isonicotinate

Synonyms:ETHYL 3-(CHLOROMETHYL)ISONICOTINATE;58553-54-1;ETHYL 3-(CHLOROMETHYL)PYRIDINE-4-CARBOXYLATE;SCHEMBL8550318;DTXSID50482493;AKOS006305334;AB60086;ETHYL3-(CHLOROMETHYL)ISONICOTINATE;FT-0732073

Suppliers and Price of Ethyl 3-(chloromethyl)isonicotinate
Supply Marketing:Edit
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
  • Crysdot
  • Ethyl3-(chloromethyl)isonicotinate 95+%
  • 1g
  • $ 681.00
  • Chemenu
  • Ethyl3-(chloromethyl)isonicotinate 95%
  • 1g
  • $ 643.00
Total 5 raw suppliers
Chemical Property of Ethyl 3-(chloromethyl)isonicotinate Edit
Chemical Property:
  • PSA:39.19000 
  • LogP:1.99710 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:199.0400063
  • Heavy Atom Count:13
  • Complexity:175
Purity/Quality:

98%min *data from raw suppliers

Ethyl3-(chloromethyl)isonicotinate 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C1=C(C=NC=C1)CCl
Technology Process of Ethyl 3-(chloromethyl)isonicotinate

There total 4 articles about Ethyl 3-(chloromethyl)isonicotinate 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:
With N-chloro-succinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; acetic acid; at 60 ℃; Irradiation;
Guidance literature:
Multi-step reaction with 3 steps
1: selenium dioxide / diphenyl ether / 1.) 155 deg C, 0.5 h , 2.) 185 deg C, 0.5 h
2: 62 percent / hydrogen chloride (gas) / 4 h / Heating
3: N-chlorosuccinimide, azobisisobutyronitrile / acetic acid; CCl4 / 60 °C / Irradiation
With hydrogenchloride; N-chloro-succinimide; selenium(IV) oxide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; diphenylether; acetic acid;
Guidance literature:
Multi-step reaction with 2 steps
1: 62 percent / hydrogen chloride (gas) / 4 h / Heating
2: N-chlorosuccinimide, azobisisobutyronitrile / acetic acid; CCl4 / 60 °C / Irradiation
With hydrogenchloride; N-chloro-succinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; acetic acid;
Refernces Edit
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