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Quinazoline, 7-bromo-2,5-dichloro-8-methoxy-

Base Information Edit
  • Chemical Name:Quinazoline, 7-bromo-2,5-dichloro-8-methoxy-
  • CAS No.:953039-88-8
  • Molecular Formula:C9H5BrCl2N2O
  • Molecular Weight:307.961
  • Hs Code.:
  • Mol file:953039-88-8.mol
Quinazoline, 7-bromo-2,5-dichloro-8-methoxy-

Synonyms:7-bromo-2,5-dichloro-8-methoxy-quinazoline

Suppliers and Price of Quinazoline, 7-bromo-2,5-dichloro-8-methoxy-
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
  • 7-Bromo-2,5-dichloro-8-methoxyquinazoline 97%
  • 1g
  • $ 589.00
  • Chemenu
  • 7-Bromo-2,5-dichloro-8-methoxyquinazoline 97%
  • 1g
  • $ 556.00
Total 2 raw suppliers
Chemical Property of Quinazoline, 7-bromo-2,5-dichloro-8-methoxy- Edit
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

7-Bromo-2,5-dichloro-8-methoxyquinazoline 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Quinazoline, 7-bromo-2,5-dichloro-8-methoxy-

There total 7 articles about Quinazoline, 7-bromo-2,5-dichloro-8-methoxy- 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 potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 16h;
Guidance literature:
Multi-step reaction with 7 steps
1.1: hydrogenchloride; iron; acetic acid / ethanol / 0.33 h / 0 °C / Heating / reflux
2.1: 1-methyl-pyrrolidin-2-one / ammonium acetate / 0.75 - 1 h / 160 °C
3.1: trichlorophosphate / 1.35 h / 0 - 145 °C / Neat (no solvent)
4.1: boron tribromide / dichloromethane / 22 h / -10 - 20 °C
4.2: 1 h / 0 °C
5.1: N-chloro-succinimide / chloroform / 2 h / 40 °C
6.1: N-Bromosuccinimide / chloroform
7.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C
With 1-methyl-pyrrolidin-2-one; hydrogenchloride; N-chloro-succinimide; N-Bromosuccinimide; boron tribromide; iron; potassium carbonate; acetic acid; trichlorophosphate; ammonium acetate; In ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 6 steps
1.1: 1-methyl-pyrrolidin-2-one / ammonium acetate / 0.75 - 1 h / 160 °C
2.1: trichlorophosphate / 1.35 h / 0 - 145 °C / Neat (no solvent)
3.1: boron tribromide / dichloromethane / 22 h / -10 - 20 °C
3.2: 1 h / 0 °C
4.1: N-chloro-succinimide / chloroform / 2 h / 40 °C
5.1: N-Bromosuccinimide / chloroform
6.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C
With 1-methyl-pyrrolidin-2-one; N-chloro-succinimide; N-Bromosuccinimide; boron tribromide; potassium carbonate; trichlorophosphate; ammonium acetate; In dichloromethane; chloroform; N,N-dimethyl-formamide;
Refernces Edit
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