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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)-

Propanoic acid, 3-(4-methoxyphenoxy)-, methyl ester

COC(=O)CCOc1ccc(cc1)OC Request for Quotation
Chemical Name: Propanoic acid, 3-(4-methoxyphenoxy)-, methyl ester
CAS Number: 18333-12-5
Product Number: AG01AIYN(AGN-PC-06FAVB)
Synonyms:
MDL No:
Molecular Formula: C11H14O4
Molecular Weight: 210.2265

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Chemical Structure


Methyl 3-(4-methoxyphenoxy)propanoate is a versatile compound commonly used in chemical synthesis as a building block for the preparation of various organic compounds. Its unique structure and properties make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. With its functional groups and reactivity, this compound can participate in a wide range of chemical reactions, including esterifications, nucleophilic substitutions, and oxidative transformations. By incorporating Methyl 3-(4-methoxyphenoxy)propanoate into synthetic pathways, chemists can access diverse molecular structures with tailored properties and functionalities for specific applications in the fields of medicine, agriculture, and materials science.