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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)-

5-Oxazolecarboxylic acid

OC(=O)c1cnco1 Request for Quotation
Chemical Name: 5-Oxazolecarboxylic acid
CAS Number: 118994-90-4
Product Number: AG0038BB(AGN-PC-00XC9L)
Synonyms:
MDL No: MFCD04114931
Molecular Formula: C4H3NO3
Molecular Weight: 113.0715

Identification/Properties

Computed Properties
Molecular Weight:
113.072g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
113.011g/mol
Monoisotopic Mass:
113.011g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
104
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

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Chemical Structure


Oxazole-5-carboxylic acid, a versatile building block in chemical synthesis, plays a crucial role in the construction of various organic compounds. With its unique molecular structure, Oxazole-5-carboxylic acid serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is often employed as a starting material for the production of heterocyclic compounds and can be further functionalized to introduce specific chemical properties. In addition, Oxazole-5-carboxylic acid exhibits valuable reactivity in the formation of complex molecules through various synthetic pathways, making it a valuable tool in the hands of synthetic chemists and researchers.