4-acetyl-2,3-dihydro-1,4-benzoxazine-2-carboxylic acid|92288-75-0,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

4-acetyl-2,3-dihydro-1,4-benzoxazine-2-carboxylic acid

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Chemical Name:	4-acetyl-2,3-dihydro-1,4-benzoxazine-2-carboxylic acid
CAS Number:	92288-75-0
Product Number:	AG006L8L(AGN-PC-0LK8WO)
Synonyms:
MDL No:
Molecular Formula:	C11H11NO4
Molecular Weight:	221.2093

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Chemical Structure

4-ACETYL-3,4-DIHYDRO-2H-BENZO[B][1,4]OXAZINE-2-CARBOXYLIC ACID, commonly employed in chemical synthesis, serves as a versatile building block and intermediate in organic chemistry. Due to its unique structure, this compound plays a crucial role in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its reactivity and functional groups make it a valuable starting material for the synthesis of complex molecules through strategic transformations such as condensation reactions, esterifications, and derivatizations. In particular, this compound is utilized in the synthesis of heterocyclic compounds, which are prevalent in medicinal chemistry and drug discovery. Its presence in the chemical toolbox enables chemists to access diverse molecular structures that exhibit potent biological activities and other desired properties.