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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)-

ethyl (2S)-2-hydroxy-3-(4-methoxyphenyl)propanoate

CCOC(=O)C(Cc1ccc(cc1)OC)O Request for Quotation
Chemical Name: ethyl (2S)-2-hydroxy-3-(4-methoxyphenyl)propanoate
CAS Number: 55301-58-1
Product Number: AG00D8D1(AGN-PC-05IZMA)
Synonyms:
MDL No:
Molecular Formula: C12H16O4
Molecular Weight: 224.2530

Identification/Properties

Properties
Storage:
Keep in dry area;-10 ℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-hydroxy-3-(4-methoxyphenyl)propanoate is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various organic molecules through esterification, condensation, or reduction reactions. In chemical synthesis, Ethyl 2-hydroxy-3-(4-methoxyphenyl)propanoate can be employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its hydroxyl group (OH) and ester functionality provide opportunities for further derivatization to introduce desired structural modifications and functional groups. Additionally, the presence of the 4-methoxyphenyl moiety enhances the compound's compatibility in certain coupling reactions, facilitating the formation of complex molecular structures.Furthermore, Ethyl 2-hydroxy-3-(4-methoxyphenyl)propanoate demonstrates good solubility in common organic solvents, enabling facile manipulation and purification during synthetic transformations. Its relatively high stability under typical reaction conditions makes it a reliable starting material for the efficient synthesis of target compounds with improved yields and selectivity.Overall, the strategic incorporation of Ethyl 2-hydroxy-3-(4-methoxyphenyl)propanoate in chemical synthesis offers practitioners a valuable tool for the construction of diverse molecular architectures with potential applications across various industries.