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3-Guanylic acid, 2-deoxy-N-(2-methyl-1-oxopropyl)-, 2-chlorophenyl 2-cyanoethyl ester

Base Information Edit
  • Chemical Name:3-Guanylic acid, 2-deoxy-N-(2-methyl-1-oxopropyl)-, 2-chlorophenyl 2-cyanoethyl ester
  • CAS No.:80817-39-6
  • Molecular Formula:C23H26ClN6O8P
  • Molecular Weight:580.922
  • Hs Code.:
  • Mol file:80817-39-6.mol
3-Guanylic acid, 2-deoxy-N-(2-methyl-1-oxopropyl)-, 2-chlorophenyl 2-cyanoethyl ester

Synonyms:

Suppliers and Price of 3-Guanylic acid, 2-deoxy-N-(2-methyl-1-oxopropyl)-, 2-chlorophenyl 2-cyanoethyl ester
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
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  • price
Total 2 raw suppliers
Chemical Property of 3-Guanylic acid, 2-deoxy-N-(2-methyl-1-oxopropyl)-, 2-chlorophenyl 2-cyanoethyl ester Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3-Guanylic acid, 2-deoxy-N-(2-methyl-1-oxopropyl)-, 2-chlorophenyl 2-cyanoethyl ester

There total 13 articles about 3-Guanylic acid, 2-deoxy-N-(2-methyl-1-oxopropyl)-, 2-chlorophenyl 2-cyanoethyl 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:
Multi-step reaction with 3 steps
1: dioxane / 2 h / 20 °C
2: 1-methylimidazole / dioxane / 3 h / 20 °C
3: benzenesulfonic acid / CHCl3; methanol / 0.25 h / 0 °C
With benzenesulfonic acid; 1-methyl-1H-imidazole; In 1,4-dioxane; methanol; chloroform;
DOI:10.1002/hlca.19820650803
Guidance literature:
Multi-step reaction with 4 steps
1: triethylamine / dioxane / 1 h / 20 °C
2: dioxane / 2 h / 20 °C
3: 1-methylimidazole / dioxane / 3 h / 20 °C
4: benzenesulfonic acid / CHCl3; methanol / 0.25 h / 0 °C
With triethylamine; benzenesulfonic acid; 1-methyl-1H-imidazole; In 1,4-dioxane; methanol; chloroform;
DOI:10.1002/hlca.19820650803
Guidance literature:
With benzenesulfonic acid; In methanol; chloroform; at 0 ℃; for 0.25h; Yield given;
DOI:10.1002/hlca.19820650803
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