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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

11,14-Eicosadienoic acid, ethyl ester, (Z,Z)-

CCCCCC=CC/C=CCCCCCCCCCC(=O)OCC Request for Quotation
Chemical Name: 11,14-Eicosadienoic acid, ethyl ester, (Z,Z)-
CAS Number: 103213-62-3
Product Number: AG00389Q(AGN-PC-0NVJQP)
Synonyms:
MDL No:
Molecular Formula: C22H40O2
Molecular Weight: 336.5518

Identification/Properties

Computed Properties
Molecular Weight:
336.56g/mol
XLogP3:
8.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
18
Exact Mass:
336.303g/mol
Monoisotopic Mass:
336.303g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
318
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
2
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


11,14-Eicosadienoic acid, ethyl ester, (11Z,14Z)-, is a versatile compound commonly used in chemical synthesis processes. This compound plays a crucial role in the creation of various organic compounds through its involvement in multiple reactions and transformations. Its unique chemical structure allows it to act as a precursor or intermediate in the synthesis of a wide range of products.In chemical synthesis, 11,14-Eicosadienoic acid, ethyl ester, (11Z,14Z)- is often utilized as a building block for the creation of complex molecules in the production of pharmaceuticals, agrochemicals, fragrances, and other fine chemicals. Its double bonds at the 11th and 14th positions enable it to participate in reactions such as hydrogenation, oxidation, and functional group transformations.Moreover, the ethyl ester form of 11,14-Eicosadienoic acid enhances its solubility and reactivity, making it a preferred choice in various synthetic processes. Its ability to undergo selective chemical modifications facilitates the creation of tailored products with specific properties and functionalities.Overall, 11,14-Eicosadienoic acid, ethyl ester, (11Z,14Z)- serves as a crucial component in the toolkit of chemists and researchers engaged in organic synthesis, providing opportunities for the development of novel compounds and materials.