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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)-

4-Oxazolecarboxylic acid, 5-phenyl-

OC(=O)c1ncoc1c1ccccc1 Request for Quotation
Chemical Name: 4-Oxazolecarboxylic acid, 5-phenyl-
CAS Number: 99924-18-2
Product Number: AG003MYE(AGN-PC-0KKXFK)
Synonyms:
MDL No: MFCD00105447
Molecular Formula: C10H7NO3
Molecular Weight: 189.1675

Identification/Properties

Properties
MP:
181 °C
BP:
354.73°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
189.17g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
189.043g/mol
Monoisotopic Mass:
189.043g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
213
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


5-Phenyloxazole-4-carboxylic acid is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic chemistry, it serves as a key building block for the synthesis of various biologically active molecules and pharmaceuticals. Through functional group transformations and derivatization, it enables the introduction of valuable structural motifs into target molecules, enhancing their pharmacological properties and potential applications. Additionally, 5-Phenyloxazole-4-carboxylic acid can also be employed in the preparation of novel materials for industrial and research purposes. Its structural characteristics make it a valuable tool for chemists seeking to access new compounds and explore innovative synthetic pathways.