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[R,E]-1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-methoxy-1-methylethyl)phenyl]propyl]thio]methyl]-cyclopropane acetic acid

Base Information
  • Chemical Name:[R,E]-1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-methoxy-1-methylethyl)phenyl]propyl]thio]methyl]-cyclopropane acetic acid
  • CAS No.:1351973-25-5
  • Molecular Formula:C36H38ClNO3S
  • Molecular Weight:600.222
  • Hs Code.:
[R,E]-1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-methoxy-1-methylethyl)phenyl]propyl]thio]methyl]-cyclopropane acetic acid

Synonyms:

Suppliers and Price of [R,E]-1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-methoxy-1-methylethyl)phenyl]propyl]thio]methyl]-cyclopropane acetic acid
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
  • MethoxyMontelukast
  • 100mg
  • $ 350.00
Total 1 raw suppliers
Chemical Property of [R,E]-1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-methoxy-1-methylethyl)phenyl]propyl]thio]methyl]-cyclopropane acetic acid
Chemical Property:
Purity/Quality:

MethoxyMontelukast *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Methoxy Montelukast is an impurity of Montelukast (M568000), a selective leukotriene D4-receptor antagonist. It is used as an antiasthmatic.
Technology Process of [R,E]-1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-methoxy-1-methylethyl)phenyl]propyl]thio]methyl]-cyclopropane acetic acid

There total 13 articles about [R,E]-1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-methoxy-1-methylethyl)phenyl]propyl]thio]methyl]-cyclopropane acetic acid 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:
Multi-step reaction with 5 steps
1.1: ethyl acetate / 25 - 30 °C
2.1: sulfuric acid; water / 5 - 10 °C
3.1: ethyl acetate / 25 - 30 °C
4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 5 °C
4.2: 2.5 h / 0 - 5 °C
5.1: water; sodium hydroxide / methanol / 5 h / 10 - 55 °C
With sulfuric acid; water; sodium hydride; sodium hydroxide; In methanol; ethyl acetate; N,N-dimethyl-formamide; mineral oil;
Guidance literature:
Multi-step reaction with 6 steps
1.1: sodium methylate / methanol; N,N-dimethyl-formamide / 0 - 5 °C
2.1: ethyl acetate / 25 - 30 °C
3.1: sulfuric acid; water / 5 - 10 °C
4.1: ethyl acetate / 25 - 30 °C
5.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 5 °C
5.2: 2.5 h / 0 - 5 °C
6.1: water; sodium hydroxide / methanol / 5 h / 10 - 55 °C
With sulfuric acid; water; sodium methylate; sodium hydride; sodium hydroxide; In methanol; ethyl acetate; N,N-dimethyl-formamide; mineral oil;
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