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Methyl 5-(chloroMethyl)nicotinate hydrochloride

Base Information
  • Chemical Name:Methyl 5-(chloroMethyl)nicotinate hydrochloride
  • CAS No.:179072-14-1
  • Molecular Formula:C8H9Cl2NO2
  • Molecular Weight:222.06856
  • Hs Code.:
  • Mol file:179072-14-1.mol
Methyl 5-(chloroMethyl)nicotinate hydrochloride

Synonyms:Methyl 5-(chloroMethyl)nicotinate hydrochloride

Suppliers and Price of Methyl 5-(chloroMethyl)nicotinate hydrochloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 9 raw suppliers
Chemical Property of Methyl 5-(chloroMethyl)nicotinate hydrochloride
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Methyl 5-(chloroMethyl)nicotinate hydrochloride

There total 5 articles about Methyl 5-(chloroMethyl)nicotinate hydrochloride 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 thionyl chloride; In dichloromethane; at 20 ℃;
Guidance literature:
Multi-step reaction with 5 steps
1: 90 percent / imidazole / dimethylformamide / 6 h / Ambient temperature
2: 1.) BuLi / 1.) THF, -78 deg C, 5 min
3: 50 percent / tetrahydrofuran; diethyl ether
4: 90 percent / NH4F / methanol / 3 h / 60 °C
5: 1.) HCl, 2.) SOCl2 / 1.) CH2Cl2, 5 min, 2.) reflux, 2 h
With 1H-imidazole; hydrogenchloride; ammonium fluoride; n-butyllithium; thionyl chloride; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1080/07328319608007388
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) BuLi / 1.) THF, -78 deg C, 5 min
2: 50 percent / tetrahydrofuran; diethyl ether
3: 90 percent / NH4F / methanol / 3 h / 60 °C
4: 1.) HCl, 2.) SOCl2 / 1.) CH2Cl2, 5 min, 2.) reflux, 2 h
With hydrogenchloride; ammonium fluoride; n-butyllithium; thionyl chloride; In tetrahydrofuran; methanol; diethyl ether;
DOI:10.1080/07328319608007388
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