Castasterone

Base Information Edit

Chemical Name:Castasterone
CAS No.:80736-41-0
Molecular Formula:C28H48 O5
Molecular Weight:464.686
Hs Code.:
DSSTox Substance ID:DTXSID7040992
Nikkaji Number:J146.604F
Wikidata:Q27109676
Metabolomics Workbench ID:34792
Mol file:80736-41-0.mol

Synonyms:24-epicastasterone;castasterone;castasterone, (2alpha,3alpha,5alpha,22R,23R)-isomer;castasterone, (2alpha,3alpha,5alpha,22S,23S)-isomer

Suppliers and Price of Castasterone

Supply Marketing:Edit

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 39 raw suppliers

Chemical Property of Castasterone Edit

Chemical Property:

Vapor Pressure:7.85E-17mmHg at 25°C
Melting Point:259-260 °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
XLogP3:4.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:464.35017463
Heavy Atom Count:33
Complexity:738

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O
Isomeric SMILES:C[C@@H]([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC(=O)[C@@H]4[C@@]3(C[C@H]([C@H](C4)O)O)C)C)[C@H]([C@@H]([C@@H](C)C(C)C)O)O
Uses Brassinolide and Castasterone were isolated from the mature seeds of smooth loofah (Luffa cylindrica (L.) M.J. Roem). A new class of plant hormones with plant growth-promothing activity.

Technology Process of Castasterone

There total 149 articles about Castasterone 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: 98.0%

: 111118-49-1
(1R,3aS,3bS,5aS,6aS,9aR,10aR,10bS,12aS)-1-{(S)-1-[(4R,5R)-5-((S)-1,2-Dimethyl-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl}-8,8,10a,12a-tetramethyl-hexadecahydro-7,9-dioxa-dicyclopenta[a,h]phenanthren-5-one

: 80736-41-0
castasterone

Guidance literature:: With trifluoroacetic acid; In methanol; for 1h;
DOI:10.1039/p19960000295

Reference yield: 94.0%

: 129824-69-7
(20S,22R,23R,24S)-23-(1-ethoxyethoxy)-6-ethylenedioxy-2α,3α-isopropylidenedioxy-5α-ergostan-22-ol

: 80736-41-0
castasterone

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; for 3h; Heating;

Reference yield: 93.0%

: 130549-19-8
Δ²-(22R,23R,24S)-22,23-dihydroxy-24-methyl-5α-cholestan-6-one

: 80736-41-0
castasterone

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In tetrahydrofuran; water; tert-butyl alcohol; for 22h; Ambient temperature;
DOI:10.1016/S0040-4020(01)85457-0