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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-Amino-1,3-oxazole-4-carboxylic acid

Nc1nc(co1)C(=O)O Request for Quotation
Chemical Name: 2-Amino-1,3-oxazole-4-carboxylic acid
CAS Number: 944900-52-1
Product Number: AG00H6CX(AGN-PC-03I9GN)
Synonyms:
MDL No:
Molecular Formula: C4H4N2O3
Molecular Weight: 128.0862

Identification/Properties

Properties
BP:
402.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
128.087g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
128.022g/mol
Monoisotopic Mass:
128.022g/mol
Topological Polar Surface Area:
89.4A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
127
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-1,3-oxazole-4-carboxylic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, $name$ is commonly used as a key starting material for the synthesis of heterocyclic compounds. Its amino and carboxylic acid functional groups can undergo a variety of transformations, allowing for the introduction of different substituents and modifications to the molecular structure. This flexibility enables the synthesis of diverse derivatives with tailored properties and functionalities.Moreover, the oxazole ring in $name$ confers additional reactivity and bioactivity to the resulting compounds, making them valuable building blocks for drug discovery and development. The presence of the amino group further enhances the potential for forming crucial chemical bonds and interactions necessary for biological activity.Overall, the application of 2-Amino-1,3-oxazole-4-carboxylic acid in chemical synthesis opens up a wide range of possibilities for the development of novel molecules with pharmacological, agricultural, and material science applications.