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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)-

2-Azetidinecarboxylic acid, 4-oxo-

O=C1CC(N1)C(=O)O Request for Quotation
Chemical Name: 2-Azetidinecarboxylic acid, 4-oxo-
CAS Number: 98019-65-9
Product Number: AG00H6MO(AGN-PC-00MOU1)
Synonyms:
MDL No:
Molecular Formula: C4H5NO3
Molecular Weight: 115.0874

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
115.088g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
115.027g/mol
Monoisotopic Mass:
115.027g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
142
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


4-Oxo-2-azetidinecarboxylic acid, also known as OACA, is a versatile building block in chemical synthesis due to its unique properties and reactivity. This compound is commonly utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, 4-Oxo-2-azetidinecarboxylic acid serves as a crucial precursor for the synthesis of heterocyclic compounds and peptides. Its four-membered azetidine ring provides structural diversity and enhances the biological activity of the final products. Additionally, the carbonyl group at the C-4 position allows for further functionalization through reactions such as esterification, amidation, and cyclization.One of the notable applications of 4-Oxo-2-azetidinecarboxylic acid is in peptide synthesis, where it acts as a pivotal component in the construction of peptide bonds. Through the activation of the carboxylic acid group using coupling reagents, such as carbodiimides or peptide coupling reagents, OACA facilitates the formation of peptide chains with high efficiency and selectivity.Furthermore, 4-Oxo-2-azetidinecarboxylic acid can be employed in the preparation of various bioactive molecules, including antiviral agents, antibiotics, and enzyme inhibitors. Its unique structure and functional groups enable chemists to modify and tailor the properties of the target compounds, leading to the development of novel therapeutics and research tools.Overall, the versatile nature of 4-Oxo-2-azetidinecarboxylic acid makes it a valuable asset in the field of chemical synthesis, offering endless possibilities for the creation of diverse organic compounds with potential applications in pharmaceuticals, agrochemicals, and beyond.