1. Home
  2. Acetic acid, [(4-methoxyphenyl)amino]oxo-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, [(4-methoxyphenyl)amino]oxo-

COc1ccc(cc1)NC(=O)C(=O)O Request for Quotation
Chemical Name: Acetic acid, [(4-methoxyphenyl)amino]oxo-
CAS Number: 41374-62-3
Product Number: AG00C6WI(AGN-PC-0LK937)
Synonyms:
MDL No:
Molecular Formula: C9H9NO4
Molecular Weight: 195.1721

Identification/Properties

Properties
MP:
215 °C (decomp)(Solv: ethanol (64-17-5))
Storage:
Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
195.174g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
195.053g/mol
Monoisotopic Mass:
195.053g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
221
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

Request for Quotation

Customer Feedback

Chemical Structure


2-((4-Methoxyphenyl)amino)-2-oxoacetic acid is a versatile compound that finds widespread application in chemical synthesis processes. Its unique chemical structure allows for various reactions and transformations, making it a valuable reagent in organic chemistry. One important use of 2-((4-Methoxyphenyl)amino)-2-oxoacetic acid is as a key intermediate in the synthesis of pharmaceutical compounds. Its ability to undergo reactions such as amide formation, ether formation, and carboxylation makes it valuable in the creation of complex drug molecules. Additionally, this compound can be utilized in the preparation of novel materials through organic reactions such as Suzuki couplings, Heck reactions, and Wittig reactions. These reactions enable the incorporation of the 2-((4-Methoxyphenyl)amino)-2-oxoacetic acid moiety into various materials with specific properties.In summary, the application of 2-((4-Methoxyphenyl)amino)-2-oxoacetic acid in chemical synthesis spans a wide range of fields, from pharmaceutical synthesis to material science, showcasing its importance as a versatile building block in organic chemistry.