ryanodol dibenzylether ketone

Base Information

Chemical Name:ryanodol dibenzylether ketone
CAS No.:127685-33-0
Molecular Formula:C₃₆H₄₄O₉
Molecular Weight:620.74
Hs Code.:

Synonyms:ryanodol dibenzylether ketone

Suppliers and Price of ryanodol dibenzylether ketone

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 0 raw suppliers

Chemical Property of ryanodol dibenzylether ketone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ryanodol dibenzylether ketone

There total 6 articles about ryanodol dibenzylether ketone 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: 60.0%

: 127685-32-9
ryanodol dibenzylether acetate

: 127685-33-0
ryanodol dibenzylether ketone

Guidance literature:: With pyridine; chromium(VI) oxide; In dichloromethane; at 25 ℃; for 0.166667h;

Reference yield:

: 6688-49-9,150736-84-8
(+)-ryanodol

: 127685-33-0
ryanodol dibenzylether ketone

Guidance literature:: Multi-step reaction with 3 steps

1: 69 percent / NaH / tetrahydrofuran; benzene / 54 h / Ambient temperature

2: 97 percent / pyridine / 30 h / 25 °C

3: 60 percent / CrO₃, pyridine / CH₂Cl₂ / 0.17 h / 25 °C

With pyridine; chromium(VI) oxide; sodium hydride; In tetrahydrofuran; dichloromethane; benzene;

Reference yield:

: 72633-76-2
epianhydroryanodol epoxide

: 127685-33-0
ryanodol dibenzylether ketone

Guidance literature:: Multi-step reaction with 4 steps

1: 60 percent / lithium / tetrahydrofuran; liquid ammonia / 1 h / -78 °C

2: 69 percent / NaH / tetrahydrofuran; benzene / 54 h / Ambient temperature

3: 97 percent / pyridine / 30 h / 25 °C

4: 60 percent / CrO₃, pyridine / CH₂Cl₂ / 0.17 h / 25 °C

With pyridine; chromium(VI) oxide; lithium; sodium hydride; In tetrahydrofuran; dichloromethane; ammonia; benzene;