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3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER

Base Information Edit
  • Chemical Name:3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER
  • CAS No.:76936-03-3
  • Molecular Formula:C32H52O3
  • Molecular Weight:484.763
  • Hs Code.:
  • Mol file:76936-03-3.mol
3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER

Synonyms:3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER

Suppliers and Price of 3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC ACID METHYL 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
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 3-METHOXY-(3-BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER 95.00%
  • 5MG
  • $ 496.52
Total 1 raw suppliers
Chemical Property of 3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER Edit
Chemical Property:
  • PSA:35.53000 
  • LogP:7.97610 
Purity/Quality:

99% *data from raw suppliers

3-METHOXY-(3-BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC ACID METHYL ESTER

There total 1 articles about 3-METHOXY-(3BETA)-OLEAN-12-EN-28-OIC 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:
Oleanolic acid; With sodium hydride; In tetrahydrofuran; at 25 ℃; for 0.25h;
methyl iodide; for 24h; Reflux; Inert atmosphere;
DOI:10.2174/1573406414666180222094544
Guidance literature:
Multi-step reaction with 3 steps
1: lithium aluminium tetrahydride / tetrahydrofuran / 24 h / -12 - 20 °C / Inert atmosphere
2: triphenylphosphine; carbon tetrabromide / acetonitrile / 7 h / 90 °C
3: lithium aluminium tetrahydride / tetrahydrofuran / 22 h / -12 - 20 °C / Reflux; Inert atmosphere
With lithium aluminium tetrahydride; carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; acetonitrile;
DOI:10.2174/1573406414666180222094544
Guidance literature:
Multi-step reaction with 3 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Reflux
2.1: pyridine; trifluoromethylsulfonic anhydride / dichloromethane / 1 h / Inert atmosphere; Cooling
2.2: 4 h / 60 °C
3.1: copper(ll) sulfate pentahydrate; sodium L-ascorbate / methanol; water / 12 h / 20 °C
With pyridine; lithium aluminium tetrahydride; copper(ll) sulfate pentahydrate; trifluoromethylsulfonic anhydride; sodium L-ascorbate; In tetrahydrofuran; methanol; dichloromethane; water;
upstream raw materials:

Oleanolic acid

methyl iodide

Downstream raw materials:

O-methyl-β-amyrin

Refernces Edit
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