Armexifolin

Base Information

Chemical Name:Armexifolin
CAS No.:64929-15-3
Molecular Formula:C₁₅H₁₈O₄
Molecular Weight:262.306
Hs Code.:
Metabolomics Workbench ID:46982
Wikidata:Q104403002
Mol file:64929-15-3.mol

Synonyms:Armexifolin;(3aS)-3abeta,5,5a,6,7,9balpha-Hexahydro-6beta-hydroxy-5aalpha,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2,8(3H,4H)-dione;1-Epiludovicin C;1-Epi-Ludovicin C;CHEBI:174461;[3aS-(3aalpha,5abeta,6beta,9bbeta)]-3a,5,5a,6,7,9b-Hexahydro-6-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2,8(3H,4H)-dione;6-hydroxy-5a,9-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9bH-naphtho[1,2-b]furan-2,8-dione;6-hydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,7,9b-hexahydrobenzo[g][1]benzouran-2,8-dione

Suppliers and Price of Armexifolin

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
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price

Total 0 raw suppliers

Chemical Property of Armexifolin

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:262.12050905
Heavy Atom Count:19
Complexity:530

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C2C3C(CCC2(C(CC1=O)O)C)C(=C)C(=O)O3

Technology Process of Armexifolin

There total 12 articles about Armexifolin 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: 100.0%

: 6-hydroxy-3,5a,9-trimethyl-3-phenylselanyl-3a,5,5a,6,7,9b-hexahydro-3H,4H-naphtho[1,2-b]furan-2,8-dione

: 64929-15-3,87550-01-4
ludovicin C

Guidance literature:: With dihydrogen peroxide; In tetrahydrofuran; water; acetic acid; at 20 ℃; for 0.5h;
DOI:10.3987/com-00-s(i)82

Reference yield:

: 59444-49-4
C₁₅H₁₈O₅

: 27740-15-4,64929-15-3,87550-01-4
ludovicin C

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / sodium benzeneselenolate, AcOH / ethanol / 0.17 h / Ambient temperature

2: 1.) lithium diisopropylamide, diphenyldiselenide; 2.) H₂O₂, AcOH / 1.) THF, -40 deg C; 2.) THF

With diphenyl diselenide; dihydrogen peroxide; sodium phenylselenide; acetic acid; lithium diisopropyl amide; In ethanol;
DOI:10.1246/cl.1987.2387

Reference yield:

: 185432-27-3
(3S,3aS,5aS,9bS)-8-Hydroxy-3,5a,9-trimethyl-3a,4,5,5a,8,9b-hexahydro-3H-naphtho[1,2-b]furan-2-one

: 27740-15-4,64929-15-3,87550-01-4
ludovicin C

Guidance literature:: Multi-step reaction with 4 steps

1: MCPBA / 0 °C

2: 88 percent / Collins reagent

3: 80 percent / sodium benzeneselenolate, AcOH / ethanol / 0.17 h / Ambient temperature

4: 1.) lithium diisopropylamide, diphenyldiselenide; 2.) H₂O₂, AcOH / 1.) THF, -40 deg C; 2.) THF

With diphenyl diselenide; dihydrogen peroxide; sodium phenylselenide; acetic acid; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; In ethanol;
DOI:10.1246/cl.1987.2387