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Ursonic acid benzyl ester

Base Information
  • Chemical Name:Ursonic acid benzyl ester
  • CAS No.:869788-71-6
  • Molecular Formula:C37H52 O3
  • Molecular Weight:544.818
  • Hs Code.:
  • Mol file:869788-71-6.mol
Ursonic acid benzyl ester

Synonyms:3-Oxo-urs-12-en-28-oic acid phenylmethyl ester;URSONIC ACID BENZYL ESTER

Suppliers and Price of Ursonic acid benzyl 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
  • American Custom Chemicals Corporation
  • URSONIC ACID BENZYL ESTER 95.00%
  • 5MG
  • $ 499.61
Total 10 raw suppliers
Chemical Property of Ursonic acid benzyl ester
Chemical Property:
  • Melting Point:156-157 °C(Solv: ethanol (64-17-5)) 
  • Boiling Point:605.3±55.0 °C(Predicted) 
  • PSA:43.37000 
  • Density:1.09±0.1 g/cm3(Predicted) 
  • LogP:8.95650 
Purity/Quality:

98%Min *data from raw suppliers

URSONIC ACID BENZYL ESTER 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Ursonic acid benzyl ester

There total 6 articles about Ursonic acid benzyl 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:
benzyl (1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,-11,12,12a,12b,13,14b-octadecahydropicene-4a(2H)-carboxylate; With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -78 - -50 ℃; for 0.25h; Inert atmosphere;
With triethylamine; In dichloromethane; at -50 - 20 ℃;
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / K2CO3 / dimethylformamide / 2 h / 85 °C
2: 89 percent / PCC / CH2Cl2 / 24 h / 0 °C
With potassium carbonate; pyridinium chlorochromate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2005.08.026
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