Austalide D

Base Information

Chemical Name:Austalide D
CAS No.:81543-04-6
Molecular Formula:C₂₈H₃₆O₁₀
Molecular Weight:532.588
Hs Code.:
Metabolomics Workbench ID:44701
Wikidata:Q105302355
Mol file:81543-04-6.mol

Synonyms:Austalide D;(1R)-1alpha-Acetyloxy-1,2,3,6,7,7a,10,14,14abeta,14b-decahydro-6alpha-hydroxy-3,13-dimethoxy-5,5,7abeta,9,14balpha-pentamethyl-12H-3beta,5abeta-epoxy-5H-furo[3,4-i]oxepino[4,3-a]xanthen-12-one;AKOS040734317;NCGC00385799-01;2-hydroxy-13,20-dimethoxy-4,7,17,22,22-pentamethyl-11-oxo-5,10,21,23-tetraoxahexacyclo[18.2.1.0^{1,17}.0^{4,16}.0^{6,14}.0^{8,12}]tricosa-6(14),7,12-trien-18-yl acetate;NCGC00385799-01_C28H36O10_2-Hydroxy-13,20-dimethoxy-4,7,17,22,22-pentamethyl-11-oxo-5,10,21,23-tetraoxahexacyclo[18.2.1.0~1,17~.0~4,16~.0~6,14~.0~8,12~]tricosa-6(14),7,12-trien-18-yl acetate

Suppliers and Price of Austalide D

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 1 raw suppliers

Chemical Property of Austalide D

Chemical Property:

Vapor Pressure:5.61E-20mmHg at 25°C
Boiling Point:689.8°Cat760mmHg
Flash Point:226.4°C
PSA：118.98000
Density:1.36g/cm³
LogP:2.95450
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:4
Exact Mass:532.23084734
Heavy Atom Count:38
Complexity:1030

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C2COC(=O)C2=C(C3=C1OC4(CC(C56C(OC(O5)(CC(C6(C4C3)C)OC(=O)C)OC)(C)C)O)C)OC

Technology Process of Austalide D

There total 1 articles about Austalide D 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:

: 33431-40-2
6-<(2E,6E)farnesyl>-5,7-dihydroxy-4-methylphthalide

: 64-17-5
ethanol

: 110925-97-8
methyl 6-ethyl-2,4-dihydroxy-3-methylbenzoate

: 110925-96-7
ethyl 6-ethyl-2,4-dihydroxy-3-methylbenzoate

: (5aR,7aS,14aR,14bS)-13-methoxy-5,5,7a,9,14b-pentamethyl-1,2,5a,6,7,7a,10,14,14a,14b-decahydro-5H-furo[3,4-i]oxepino[4,3-a]xanthene-3,12-dione

: 81543-04-6
austalide D

Guidance literature:: With Aspergillus ustis (3-day old, yellow maize meal); for 288h; Mechanism; incorporation of different labelled acetates, (3RS)-mevalonolactones and (2S)-methionine and other mediums; with and without ethanol or methanol;