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cycloprotobuxine A

Base Information
  • Chemical Name:cycloprotobuxine A
  • CAS No.:2278-38-8
  • Molecular Formula:C28H50N2
  • Molecular Weight:414.718
  • Hs Code.:
  • Mol file:2278-38-8.mol
cycloprotobuxine A

Synonyms:9,19-Cyclo-5a,9b-pregnane-3b,20a-diamine, N3,N3,N20,N20,4,4,14-heptamethyl- (8CI); Cycloprotobuxine A(7CI); 1H,19H-Cyclopropa[9,10]cyclopenta[a]phenanthrene,9,19-cyclopregnane-3,20-diamine deriv.

Suppliers and Price of cycloprotobuxine A
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
  • CYCLOPROTOBUXINE A 95.00%
  • 5MG
  • $ 497.59
Total 4 raw suppliers
Chemical Property of cycloprotobuxine A
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:472.2°Cat760mmHg 
  • Flash Point:206.2°C 
  • PSA:6.48000 
  • Density:1g/cm3 
  • LogP:6.30580 
Purity/Quality:

99% *data from raw suppliers

CYCLOPROTOBUXINE A 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of cycloprotobuxine A

There total 11 articles about cycloprotobuxine A 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: 90 percent / hydroxylamine hydrochloride, pyridine / 4 h / Heating
2: 1.096 g / lithium aluminium hydride / dioxane / 20 h / Heating
3: 11 percent / 85 percent formic acid / dioxane; H2O / 24 h / Heating
With pyridine; lithium aluminium tetrahydride; formic acid; hydroxylamine hydrochloride; In 1,4-dioxane; water;
DOI:10.1016/S0040-4020(01)96027-2
Guidance literature:
Multi-step reaction with 4 steps
1: 90 percent / Jones reagent / acetone / 0 °C
2: 90 percent / hydroxylamine hydrochloride, pyridine / 4 h / Heating
3: 1.096 g / lithium aluminium hydride / dioxane / 20 h / Heating
4: 11 percent / 85 percent formic acid / dioxane; H2O / 24 h / Heating
With pyridine; lithium aluminium tetrahydride; formic acid; jones reagent; hydroxylamine hydrochloride; In 1,4-dioxane; water; acetone;
DOI:10.1016/S0040-4020(01)96027-2
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