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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)-

ω-3 Arachidonic Acid methyl ester

CC/C=CC/C=CC/C=CC/C=CCCCCCCC(=O)OC Request for Quotation
Chemical Name: ω-3 Arachidonic Acid methyl ester
CAS Number: 132712-70-0
Product Number: AG00111O(AGN-PC-0WAIB7)
Synonyms:
MDL No:
Molecular Formula: C21H34O2
Molecular Weight: 318.4935

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Chemical Structure


In chemical synthesis, ω-3 Arachidonic Acid methyl ester serves as a valuable reagent due to its unique properties and functional groups. This compound can be utilized as a precursor for the preparation of various derivatives and analogs through reactions such as esterification, hydrolysis, and alkylation. Its omega-3 fatty acid structure makes it particularly useful in the synthesis of bioactive compounds and pharmaceutical intermediates. With its potential to undergo selective functional group transformations, ω-3 Arachidonic Acid methyl ester plays a crucial role in the development of new chemical entities and research in the field of organic chemistry.