Anthiaergostan-5,7,9,22-tetraen-3-one

Base Information

Chemical Name:Anthiaergostan-5,7,9,22-tetraen-3-one
CAS No.:64110-74-3
Molecular Formula:C₂₈H₄₀O
Molecular Weight:392.625
Hs Code.:

Synonyms:1H-Cyclopent[a]anthracen-8(2H)-one,3,3a,4,5,7,9,10,11b-octahydro-3a,6-dimethyl-3-(1,4,5-trimethyl-2-hexenyl)-(7CI); 8H-Cyclopent[a]anthracene,1,6-cyclo-1,10-secoergosta-5,7,9,22-tetraen-3-one deriv.

Suppliers and Price of Anthiaergostan-5,7,9,22-tetraen-3-one

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 3 raw suppliers

Chemical Property of Anthiaergostan-5,7,9,22-tetraen-3-one

Chemical Property:

Boiling Point:509.0±39.0 °C(Predicted)
PSA：17.07000
Density:1.005±0.06 g/cm3(Predicted)
LogP:6.98330

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Anthiaergostan-5,7,9,22-tetraen-3-one

There total 5 articles about Anthiaergostan-5,7,9,22-tetraen-3-one 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:

: 474-71-5,601-45-6,23454-50-4
ergosta-5,7,22-trien-3-one

: 64110-74-3
1(10->6)abeo-ergosta-5,7,9,22-tetraen-3-one

Guidance literature:: Multi-step reaction with 4 steps

2: 1.1 g / sodium borohydride / methanol; CHCl₃ / 2 h / Ambient temperature

3: 0.17 g / boron trifluoride-ether / benzene / 4.5 h / Ambient temperature; more rapid (10 min) conversion for benzoate; other adduct of steroidal 5.7-dienes with 4-phenyl-1,2,4-triazoline-3,5-dione

4: Moffatt reagent

With sodium tetrahydroborate; Moffatt reagent; boron trifluoride diethyl etherate; In methanol; chloroform; benzene;

Reference yield:

: 64110-28-7
C₃₆H₄₇N₃O₃

: 64110-74-3
1(10->6)abeo-ergosta-5,7,9,22-tetraen-3-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1.1 g / sodium borohydride / methanol; CHCl₃ / 2 h / Ambient temperature

2: 0.17 g / boron trifluoride-ether / benzene / 4.5 h / Ambient temperature; more rapid (10 min) conversion for benzoate; other adduct of steroidal 5.7-dienes with 4-phenyl-1,2,4-triazoline-3,5-dione

3: Moffatt reagent

With sodium tetrahydroborate; Moffatt reagent; boron trifluoride diethyl etherate; In methanol; chloroform; benzene;

Reference yield:

: 10123-90-7,76035-89-7,137174-33-5
C₃₆H₄₉N₃O₃

: 64110-74-3
1(10->6)abeo-ergosta-5,7,9,22-tetraen-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 0.17 g / boron trifluoride-ether / benzene / 4.5 h / Ambient temperature; more rapid (10 min) conversion for benzoate; other adduct of steroidal 5.7-dienes with 4-phenyl-1,2,4-triazoline-3,5-dione

2: Moffatt reagent

With Moffatt reagent; boron trifluoride diethyl etherate; In benzene;