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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)-

Acetic acid, oxo(phenylamino)-, ethyl ester

CCOC(=O)C(=O)Nc1ccccc1 Request for Quotation
Chemical Name: Acetic acid, oxo(phenylamino)-, ethyl ester
CAS Number: 1457-85-8
Product Number: AG001DBU(AGN-PC-0JLB7U)
Synonyms:
MDL No:
Molecular Formula: C10H11NO3
Molecular Weight: 193.1992

Identification/Properties

Properties
MP:
67-69 °C(lit.)
BP:
280.0°C
Storage:
Room Temperature;
Form:
Solid
Refractive Index:
1.5300 (estimate)
Computed Properties
Molecular Weight:
193.202g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
193.074g/mol
Monoisotopic Mass:
193.074g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
209
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-oxo-2-(phenylamino)acetate is a versatile compound widely used in chemical synthesis for its ability to participate in various reactions and transformations. This compound is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique chemical properties.In chemical synthesis, Ethyl 2-oxo-2-(phenylamino)acetate serves as a valuable building block in the formation of complex molecules. Its keto and amino functional groups make it a valuable substrate for various reactions such as nucleophilic addition, condensation, and cyclization. By reacting with different reagents and catalysts, this compound can be transformed into a wide range of structurally diverse compounds with different pharmacological or chemical properties.Furthermore, Ethyl 2-oxo-2-(phenylamino)acetate can undergo various functional group transformations, such as acylation, alkylation, and oxidation, to introduce new functionalities into the molecule. This versatility allows chemists to tailor the structure of the final product to achieve specific properties or activities desired for a particular application.Overall, Ethyl 2-oxo-2-(phenylamino)acetate plays a crucial role in the field of chemical synthesis by serving as a key intermediate for the construction of complex molecules with important applications in the pharmaceutical, agricultural, and chemical industries.