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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)-

ethyl 5-(4-methoxyphenyl)-1,2-oxazole-3-carboxylate

CCOC(=O)c1noc(c1)c1ccc(cc1)OC Request for Quotation
Chemical Name: ethyl 5-(4-methoxyphenyl)-1,2-oxazole-3-carboxylate
CAS Number: 925006-96-8
Product Number: AG00IH6G(AGN-PC-0NMOWS)
Synonyms:
MDL No:
Molecular Formula: C13H13NO4
Molecular Weight: 247.2466

Identification/Properties

Computed Properties
Molecular Weight:
247.25g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
247.084g/mol
Monoisotopic Mass:
247.084g/mol
Topological Polar Surface Area:
61.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
276
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The Ethyl 5-(4-methoxyphenyl)isoxazole-3-carboxylate compound plays a crucial role in chemical synthesis as a versatile building block for the creation of novel molecules. Its functional groups offer strategic points for derivatization, enabling the synthesis of diverse chemical structures with various properties and applications. In organic synthesis, this compound can serve as a key intermediate in the construction of pharmaceuticals, agrochemicals, and materials with desired characteristics. By leveraging the reactivity of the isoxazole ring and the ester functionality, chemists can efficiently access structurally complex compounds through sequential transformations. Its presence in the synthesis pathway can lead to the formation of bioactive compounds or advanced materials with tailored functionalities, making it a valuable tool for chemical researchers seeking to expand the scope of molecular design.