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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)-

Methyl 4-(5-Oxazolyl)benzoate

COC(=O)c1ccc(cc1)c1ocnc1 Request for Quotation
Chemical Name: Methyl 4-(5-Oxazolyl)benzoate
CAS Number: 179057-14-8
Product Number: AG0026QO(AGN-PC-0K5RWS)
Synonyms:
MDL No: MFCD03012557
Molecular Formula: C11H9NO3
Molecular Weight: 203.1941

Identification/Properties

Properties
MP:
112～114℃
BP:
341.5±25.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
203.197g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
203.058g/mol
Monoisotopic Mass:
203.058g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
224
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 4-(5-oxazolyl)benzoate, a versatile compound frequently utilized in chemical synthesis, serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it highly valuable in organic chemistry processes, specifically in the formation of heterocyclic compounds and the modification of aromatic systems. By incorporating this compound into synthetic pathways, chemists can access a wide range of derivatives with diverse properties and applications. Additionally, the presence of the oxazole ring confers specific biological activities to the resulting molecules, making them of great interest in medicinal chemistry research.