Isooblusilactonc A

Base Information

Chemical Name:Isooblusilactonc A
CAS No.:56522-16-8
Molecular Formula:C19H32O3
Molecular Weight:308.4556
Hs Code.:
Wikidata:Q104993216
Metabolomics Workbench ID:134729
ChEMBL ID:CHEMBL449423

Synonyms:Isooblusilactonc A;56522-16-8;CHEMBL449423;2(3H)-Furanone, dihydro-4-hydroxy-5-methylene-3-tetradecylidene-, (3E,4S)-

Suppliers and Price of Isooblusilactonc A

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 Isooblusilactonc A

Chemical Property:

Vapor Pressure:2.6E-10mmHg at 25°C
Boiling Point:457.9°C at 760 mmHg
Flash Point:181°C
Density:0.98g/cm³
XLogP3:6.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:12
Exact Mass:308.23514488
Heavy Atom Count:22
Complexity:371

Purity/Quality:: ≥98% （HPLC） ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O
Isomeric SMILES:CCCCCCCCCCCCC/C=C/1\[C@@H](C(=C)OC1=O)O

Technology Process of Isooblusilactonc A

There total 8 articles about Isooblusilactonc A 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: 46.0%

: 78277-61-9
(E)-2-(1-Hydroxy-prop-2-ynyl)-hexadec-2-enoic acid

: 56522-15-7,56522-16-8,71242-34-7
(+/-)-isoobtusilactone A

Guidance literature:: With mercury(II) trifluoroacetate; In dichloromethane; at 0 ℃; for 2h; further reagent;
DOI:10.1021/ja00404a023

Reference yield: 18.0%

: 78277-64-2
(Z)-2-(1-Hydroxy-prop-2-ynyl)-hexadec-2-enoic acid

: 56522-15-7,56522-16-8,71242-34-7
(+/-)-obtusilactone A

Guidance literature:: With mercury(II) trifluoroacetate; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1021/ja00404a023

Reference yield:

: 112-39-0
hexadecanoic acid methyl ester

: 56522-15-7,56522-16-8,71242-34-7
(+/-)-obtusilactone A

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) lithium diisopropylamide / 1.) THF, -78 deg C, 1 h, 2.) -78 deg C -> room temperature, 30 min

2: 1.) lithium diisopropylamide, 2.) hydrogen peroxide, acetic acid / 1.) THF, -78 deg C, 20 min, 2.) 0 deg C, 30 min, room temperature, 2 h

3: 98 percent / KOH / methanol; H₂O / 2 h / 25 °C

4: 18 percent / mercuric trifluoroacetate / CH₂Cl₂ / 2 h / 0 °C

With potassium hydroxide; dihydrogen peroxide; mercury(II) trifluoroacetate; acetic acid; lithium diisopropyl amide; In methanol; dichloromethane; water;
DOI:10.1021/ja00404a023