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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)-

methyl 2-oxo-3-phenylbutanoate

COC(=O)C(=O)C(c1ccccc1)C Request for Quotation
Chemical Name: methyl 2-oxo-3-phenylbutanoate
CAS Number: 65499-01-6
Product Number: AG00IBI1(AGN-PC-0005RJ)
Synonyms:
MDL No:
Molecular Formula: C11H12O3
Molecular Weight: 192.21118

Identification/Properties

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


Methyl 2-oxo-3-phenylbutanoate is commonly used in chemical synthesis as a key building block for the creation of various compounds. Its unique chemical structure makes it a versatile reagent in organic reactions, particularly in the formation of pharmaceutical intermediates and fine chemicals. This compound serves as a valuable starting material in the preparation of esters, amides, and other complex molecules due to its ability to participate in diverse synthetic transformations. Its strategic placement of functional groups enables efficient derivatization to access a wide range of molecular architectures, making it a valuable tool for synthetic chemists seeking to construct structurally complex compounds efficiently and effectively.