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20-ethyl-8,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate

Base Information
  • Chemical Name:20-ethyl-8,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate
  • CAS No.:91794-14-8
  • Molecular Formula:C33H47NO9
  • Molecular Weight:601.737
  • Hs Code.:
20-ethyl-8,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate

Synonyms:2H-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine,aconitane-8,13,14-triol deriv.; Bikhaconine 14-p-methoxybenzoate; Forestine

Suppliers and Price of 20-ethyl-8,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate
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
  • Forestine
  • 50mg
  • $ 1055.00
  • TRC
  • Forestine
  • 5mg
  • $ 130.00
Total 4 raw suppliers
Chemical Property of 20-ethyl-8,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate
Chemical Property:
  • Vapor Pressure:7.29E-20mmHg at 25°C 
  • Boiling Point:687.8°C at 760 mmHg 
  • Flash Point:369.8°C 
  • Density:1.31g/cm3 
Purity/Quality:

96.0% *data from raw suppliers

Forestine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Forestine is known diterprenoid alkaloid isolated from Aconitum crassicaule and it is used in the study of plant biochemistry and biology.
Technology Process of 20-ethyl-8,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate

There total 1 articles about 20-ethyl-8,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate 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:

Reference yield: 98.0%

Guidance literature:
With water; In 1,4-dioxane; Reflux;
DOI:10.1248/cpb.57.801
Guidance literature:
With pyridine; dmap; Reflux;
DOI:10.1248/cpb.57.801
Guidance literature:
With pyridine; dmap; Reflux;
DOI:10.1248/cpb.57.801
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