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3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester

Base Information
  • Chemical Name:3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester
  • CAS No.:1092568-87-0
  • Molecular Formula:C12H10N2O3
  • Molecular Weight:230.223
  • Hs Code.:
  • Mol file:1092568-87-0.mol
3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester

Synonyms:3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester;methyl 3-(5-hydroxypyrimidin-2-yl)benzoate

Suppliers and Price of 3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester
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
  • Chemenu
  • 3-(5-Hydroxypyrimidin-2-yl)benzoicacidmethylester 95%+
  • 100mg
  • $ 737.00
  • A1 Biochem Labs
  • Methyl3-(5-hydroxypyrimidin-2-yl)benzoate 95%
  • 2.5 g
  • $ 1100.00
Total 17 raw suppliers
Chemical Property of 3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester
Chemical Property:
  • PSA:72.31000 
  • LogP:1.63580 
Purity/Quality:

99%, *data from raw suppliers

3-(5-Hydroxypyrimidin-2-yl)benzoicacidmethylester 95%+ *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester

There total 9 articles about 3-(5-HydroxypyriMidin-2-yl)benzoic acid Methyl ester 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 sodium hydrogencarbonate; potassium carbonate; In diethyl ether; ethyl acetate;
Guidance literature:
Multi-step reaction with 4 steps
1: hydrogen; water; acetic acid / Raney nickel / methanol / 18 h / 20 °C / 760.05 Torr
2: sodium methylate / methanol / 1.17 h / 60 °C
3: water; sulfuric acid / 4 h / Reflux
4: thionyl chloride / 6 h / 80 °C
With thionyl chloride; sulfuric acid; water; hydrogen; sodium methylate; acetic acid; Raney nickel; In methanol;
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