2-(2-ethyl-6-methylanilino)-2-oxoacetic acid


Chemical Name: 2-(2-ethyl-6-methylanilino)-2-oxoacetic acid
CAS Number: 152019-74-4
Product Number: AG007JSL(AGN-PC-05EGSV)
Synonyms:
MDL No:
Molecular Formula: C11H13NO3
Molecular Weight: 207.2258

Identification/Properties


Computed Properties
Molecular Weight:
207.229g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
207.09g/mol
Monoisotopic Mass:
207.09g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
252
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

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Chemical Structure



The compound 2-((2-Ethyl-6-methylphenyl)amino)-2-oxoacetic acid, also known as $name$, is a versatile chemical reagent commonly used in chemical synthesis processes. Its unique structure and properties make it a valuable tool in various organic reactions and transformations.$name$ can serve as a key building block in the synthesis of complex organic compounds due to its ability to undergo a range of chemical reactions. Its amino and oxoacetic acid functional groups allow for selective modifications, enabling the introduction of new functionalities or structural motifs into target molecules. In chemical synthesis, $name$ is often employed as a nucleophilic or electrophilic agent, participating in processes such as acylation, amidation, and condensation reactions. Its presence can facilitate the formation of peptide bonds, ester linkages, and other important chemical bonds essential for the creation of biologically active compounds, pharmaceuticals, and materials.Furthermore, $name$ can act as a catalyst or a reactant in various synthetic pathways, promoting the formation of desired products by controlling reaction kinetics and selectivity. Its role in mediating chemical transformations makes it a valuable asset in the laboratory for constructing novel organic structures with tailored properties and functions.Overall, the application of 2-((2-Ethyl-6-methylphenyl)amino)-2-oxoacetic acid in chemical synthesis spans a wide range of reactions and processes, making it an indispensable tool for organic chemists and researchers working to develop new molecules and materials for diverse applications.