EPICASTASTERONE

Base Information

Chemical Name:EPICASTASTERONE
CAS No.:72050-71-6
Molecular Formula:C28H48 O5
Molecular Weight:464.686
Hs Code.:

Synonyms:24-Epicastasterone;24-epi-Castasterone; 24R-Epicastasterone

Suppliers and Price of EPICASTASTERONE

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

TRC
24-epi-Castasterone
250mg
$ 1175.00

Total 6 raw suppliers

Chemical Property of EPICASTASTERONE

Chemical Property:

Vapor Pressure:7.85E-17mmHg at 25°C
Melting Point:241-245 °C
Boiling Point:598.7°C at 760 mmHg
PKA:14.29±0.20(Predicted)
Flash Point:329.9°C
PSA：97.99000
Density:1.127g/cm³
LogP:3.80600

Purity/Quality:

97% ^*data from raw suppliers

24-epi-Castasterone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses A metabolite of Castasterone (C226500). An 24-epimer of Castasterone.

Technology Process of EPICASTASTERONE

There total 20 articles about EPICASTASTERONE 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:

: 72050-69-2,72050-71-6,80736-41-0,80736-42-1,110416-32-5,113666-78-7,121398-05-8,121468-14-2,121468-15-3,121468-16-4,135559-13-6,147200-30-4,147200-31-5
(2R,3S,5S,17R)-17-((1S,4R)-2,3-Dihydroxy-1,4,5-trimethyl-hexyl)-2,3-dihydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-6-one

Guidance literature:: Dien 7, OsO4;
DOI:10.1021/jo00394a066

Reference yield:

: 72050-69-2,72050-71-6,80736-41-0,80736-42-1,110416-32-5,113666-78-7,121398-05-8,121468-14-2,121468-15-3,121468-16-4,135559-13-6,147200-30-4,147200-31-5
(2R,3S,5S,10R,13S,17R)-17-((1S,2S,3S,4R)-2,3-Dihydroxy-1,4,5-trimethyl-hexyl)-2,3-dihydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-6-one

Guidance literature:: Dien 7, OsO4;
DOI:10.1021/jo00394a066

Reference yield:

: 57-87-4
Ergosterol

: 72050-69-2,72050-71-6,80736-41-0,80736-42-1,110416-32-5,113666-78-7,121398-05-8,121468-14-2,121468-15-3,121468-16-4,135559-13-6,147200-30-4,147200-31-5
(22S,23S,24R)-2α,3α,22,23-tetrahydroxy-5α-ergostan-6-one

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine / Ambient temperature

2: water, potassium hydrocarbonate / acetone

3: CrO₃, pyridine

4: 94 percent / Li, liq. NH₃ / diethyl ether / 0.08 h / -70 - -60 °C

5: 72 percent / pyridine hydrobromide / dimethylformamide / Heating

6: OsO₄

With pyridine; chromium(VI) oxide; osmium(VIII) oxide; ammonia; water; Pyridine hydrobromide; lithium; potassium hydrogencarbonate; In diethyl ether; N,N-dimethyl-formamide; acetone;