(5Z,8Z,11Z)-13-((2R,3S)-3-pentyloxiran-2-yl)trideca-5,8,11-trienoic acid

Base Information Edit

Chemical Name:(5Z,8Z,11Z)-13-((2R,3S)-3-pentyloxiran-2-yl)trideca-5,8,11-trienoic acid
CAS No.:105304-92-5
Molecular Formula:C₂₀H₃₂O₃
Molecular Weight:320.472
Hs Code.:2918990090
European Community (EC) Number:631-283-4
Mol file:105304-92-5.mol

Synonyms:14(R),15(S)-Epoxy-(5Z,8Z,11Z)-eicosatrienoic acid;(5Z,8Z,11Z)-13-((2R,3S)-3-pentyloxiran-2-yl)trideca-5,8,11-trienoic acid;105304-92-5

Suppliers and Price of (5Z,8Z,11Z)-13-((2R,3S)-3-pentyloxiran-2-yl)trideca-5,8,11-trienoic acid

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

Cayman Chemical
14S(15R)-EET
100μg
$ 693.00

Cayman Chemical
14S(15R)-EET
50μg
$ 421.00

Cayman Chemical
14S(15R)-EET
25μg
$ 235.00

Cayman Chemical
14S(15R)-EET
10μg
$ 99.00

Total 3 raw suppliers

Chemical Property of (5Z,8Z,11Z)-13-((2R,3S)-3-pentyloxiran-2-yl)trideca-5,8,11-trienoic acid Edit

Chemical Property:

Vapor Pressure:6.48E-10mmHg at 25°C
Refractive Index:1.501
Boiling Point:464.5°C at 760 mmHg
Flash Point:155.7°C
PSA：49.83000
Density:0.983g/cm³
LogP:5.42790
Storage Temp.:−20°C
XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:14
Exact Mass:320.23514488
Heavy Atom Count:23
Complexity:396

Purity/Quality:

98%Min ^*data from raw suppliers

14S(15R)-EET ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:F,Xi
Statements: 11-36/37/38
Safety Statements: 16-26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC1C(O1)CC=CCC=CCC=CCCCC(=O)O
Isomeric SMILES:CCCCC[C@H]1[C@H](O1)CC=CCC=CCC=CCCCC(=O)O

Technology Process of (5Z,8Z,11Z)-13-((2R,3S)-3-pentyloxiran-2-yl)trideca-5,8,11-trienoic acid

There total 8 articles about (5Z,8Z,11Z)-13-((2R,3S)-3-pentyloxiran-2-yl)trideca-5,8,11-trienoic acid 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:

: 506-32-1,236743-58-1
all cis 5,8,11,14-eicosatetraenoic acid

: 105304-92-5,81276-03-1
14(S),15(R)-Epoxyeicosatrienoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: cytochrome P₄₅₀BM₃ (F₈₇V); NADPH; K₂CO₃ / various solvent(s) / 0.25 h / 20 °C / pH 7.4

1.2: 45 percent / diethyl ether; methanol

2.1: NaOH / tetrahydrofuran; H₂O / 6 h / 23 °C

2.2: HCl / tetrahydrofuran; H₂O / pH 4.5

With sodium hydroxide; cytochrome P₄₅₀BM₃ (F₈₇V); potassium carbonate; NADPH; In tetrahydrofuran; water;
DOI:10.1016/S0040-4039(01)00694-3