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6-bromo-4-chloro-7-methoxycinnoline-3-carboxamide

Base Information
  • Chemical Name:6-bromo-4-chloro-7-methoxycinnoline-3-carboxamide
  • CAS No.:1041853-24-0
  • Molecular Formula:C10H7 Br Cl N3 O2
  • Molecular Weight:316.541
  • Hs Code.:
  • Mol file:1041853-24-0.mol
6-bromo-4-chloro-7-methoxycinnoline-3-carboxamide

Synonyms:

Suppliers and Price of 6-bromo-4-chloro-7-methoxycinnoline-3-carboxamide
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
  • SynChem
  • 6-Bromo-4-chloro-7-methoxycinnoline-3-carboxylic acid amide 95+%
  • 5 g
  • $ 1185.00
  • SynChem
  • 6-Bromo-4-chloro-7-methoxycinnoline-3-carboxylic acid amide 95+%
  • 1 g
  • $ 295.00
Total 6 raw suppliers
Chemical Property of 6-bromo-4-chloro-7-methoxycinnoline-3-carboxamide
Chemical Property:
  • PSA:79.09000 
  • LogP:3.03740 
Purity/Quality:

98%min *data from raw suppliers

6-Bromo-4-chloro-7-methoxycinnoline-3-carboxylic acid amide 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 6-bromo-4-chloro-7-methoxycinnoline-3-carboxamide

There total 5 articles about 6-bromo-4-chloro-7-methoxycinnoline-3-carboxamide 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:
6-bromo-4-hydroxy-7-methoxycinnoline-3-carboxylic acid; With thionyl chloride; N,N-dimethyl-formamide; for 4h; Heating / reflux;
With ammonia; In water; acetone; at 0 ℃; for 0.25h;
Guidance literature:
Multi-step reaction with 2 steps
1.1: potassium hydroxide / ethanol; water / Reflux
2.1: thionyl chloride; N,N-dimethyl-formamide / Reflux
2.2: 0 °C
With thionyl chloride; N,N-dimethyl-formamide; potassium hydroxide; In ethanol; water;
DOI:10.1016/j.bmcl.2011.01.033
Guidance literature:
Multi-step reaction with 4 steps
1.1: hydrogenchloride; sodium nitrite / water / 0 °C
1.2: 20 °C
2.1: titanium tetrachloride / toluene / Reflux
3.1: potassium hydroxide / ethanol; water / Reflux
4.1: thionyl chloride; N,N-dimethyl-formamide / Reflux
4.2: 0 °C
With hydrogenchloride; thionyl chloride; titanium tetrachloride; N,N-dimethyl-formamide; potassium hydroxide; sodium nitrite; In ethanol; water; toluene;
DOI:10.1016/j.bmcl.2011.01.033
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