Prostephanaberrine

Base Information

Chemical Name:Prostephanaberrine
CAS No.:105608-27-3
Molecular Formula:C₁₉H₂₁NO₅
Molecular Weight:343.379
Hs Code.:
Mol file:105608-27-3.mol

Synonyms:3a,10b-[2]Buteno-1H-[1,3]benzodioxolo[5,6-e]indole,hasubanan-8-one deriv.; (-)-Prostephanaberrine; Base B, from Stephaniajaponica; Prostephanaberrine

Suppliers and Price of Prostephanaberrine

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

Crysdot
Prostephanaberrine 95+%
5mg
$ 998.00

Arctom
Prostephanaberrine
5mg
$ 643.00

Total 11 raw suppliers

Chemical Property of Prostephanaberrine

Chemical Property:

Vapor Pressure:4.63E-12mmHg at 25°C
Boiling Point:530°Cat760mmHg
Flash Point:274.3°C
PSA：68.23000
Density:1.42g/cm³
LogP:1.60550

Purity/Quality:

97.00% ^*data from raw suppliers

Prostephanaberrine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Prostephanaberrine

There total 3 articles about Prostephanaberrine 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: 85.0%

: C₁₉H₂₃NO₆

: 105608-27-3
(-)-prostephanaberrine

Guidance literature:: With sodium ethanolate; In ethanol; at 75 ℃; for 0.333333h; Inert atmosphere;
DOI:10.1021/jo401889b

Reference yield:

: 1025023-05-5
(7β,8β,10β)-8,10-epoxy-7,8-dimethoxy-2,3-[methylenebis(oxy)]-17-methyl-6-oxohasubanan

: 105608-27-3
(-)-prostephanaberrine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate / ethanol / 0.25 h / 0 °C / Inert atmosphere

2: hydrogenchloride / water / 4 h / 75 °C / Inert atmosphere

3: sodium ethanolate / ethanol / 0.33 h / 75 °C / Inert atmosphere

With hydrogenchloride; sodium tetrahydroborate; sodium ethanolate; In ethanol; water;
DOI:10.1021/jo401889b

Reference yield:

: C₂₀H₂₃NO₆

: 105608-27-3
(-)-prostephanaberrine

Guidance literature:: Multi-step reaction with 4 steps

1: formic acid / Inert atmosphere

2: sodium tetrahydroborate / ethanol / 0.25 h / 0 °C / Inert atmosphere

3: hydrogenchloride / water / 4 h / 75 °C / Inert atmosphere

4: sodium ethanolate / ethanol / 0.33 h / 75 °C / Inert atmosphere

With hydrogenchloride; sodium tetrahydroborate; formic acid; sodium ethanolate; In ethanol; water;
DOI:10.1021/jo401889b