ervayunine

Base Information

Chemical Name:ervayunine
CAS No.:120202-64-4
Molecular Formula:C₁₉H₂₄N₂O
Molecular Weight:296.412
Hs Code.:
Mol file:120202-64-4.mol

Synonyms:2H-3,13-Methanooxireno[9,10]azacycloundecino[5,4-b]indole,13-ethyl-1a,4,5,10,11,12,13,13a-octahydro-, (1aS,13R,13aR)- (9CI);2H-3,13-Methanooxireno[9,10]azacycloundecino[5,4-b]indole,13-ethyl-1a,4,5,10,11,12,13,13a-octahydro-, [1aS-(1aR*,13S*,13aS*)]-;(-)-Ervayunine; Ervayunine

Suppliers and Price of ervayunine

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

Total 1 raw suppliers

Chemical Property of ervayunine

Chemical Property:

Vapor Pressure:1.12E-08mmHg at 25°C
Boiling Point:460.9°Cat760mmHg
Flash Point:232.5°C
PSA：31.56000
Density:1.22g/cm³
LogP:3.07390

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of ervayunine

There total 6 articles about ervayunine 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: 80.0%

: 475147-84-3
(-)-1,2-didehydro-(14R,15S)-epoxy-aspidospermidine

: 120202-64-4,15266-46-3
voaphylline

Guidance literature:: With sodium tetrahydroborate; In ethanol; for 1h; Heating;
DOI:10.1021/jo020386r

Reference yield:

: (-)-14,15-didehydroaspidospermidine

: 120202-64-4,15266-46-3
voaphylline

Guidance literature:: Multi-step reaction with 5 steps

1: 88 percent / CH₂Cl₂ / 24 h / 20 °C

2: 79 percent / HClO₄; m-chloroperoxy-benzoic acid / methanol / 0 - 20 °C

3: 55 percent / Zn / methanol / 18 h / Heating

4: 39 percent / potassium permanagnate; 18-crown-6 ether / benzene / 2 h / 20 °C

5: 80 percent / NaBH₄ / ethanol / 1 h / Heating

With sodium tetrahydroborate; potassium permanganate; perchloric acid; 18-crown-6 ether; 3-chloro-benzenecarboperoxoic acid; zinc; In methanol; ethanol; dichloromethane; benzene;
DOI:10.1021/jo020386r

Reference yield:

: 475147-83-2
(-)-(14R,15S)-epoxy-aspidospermidine

: 120202-64-4,15266-46-3
voaphylline

Guidance literature:: Multi-step reaction with 2 steps

1: 39 percent / potassium permanagnate; 18-crown-6 ether / benzene / 2 h / 20 °C

2: 80 percent / NaBH₄ / ethanol / 1 h / Heating

With sodium tetrahydroborate; potassium permanganate; 18-crown-6 ether; In ethanol; benzene;
DOI:10.1021/jo020386r