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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-(4-chlorophenyl)-1,2-oxazole-5-carboxylate

COC(=O)c1oncc1c1ccc(cc1)Cl Request for Quotation
Chemical Name: methyl 4-(4-chlorophenyl)-1,2-oxazole-5-carboxylate
CAS Number: 1072944-87-6
Product Number: AG003RTN(AGN-PC-07XU3Y)
Synonyms:
MDL No:
Molecular Formula: C11H8ClNO3
Molecular Weight: 237.6391

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
237.639g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
237.019g/mol
Monoisotopic Mass:
237.019g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
254
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 4-(4-chlorophenyl)isoxazole-5-carboxylate is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity allow for the introduction of the isoxazole moiety into organic molecules, opening up a myriad of opportunities for the development of new compounds with desirable properties. In chemical synthesis, Methyl 4-(4-chlorophenyl)isoxazole-5-carboxylate can undergo various reactions, such as nucleophilic substitution, acylation, and condensation, facilitating the formation of complex molecular structures. Researchers and chemists utilize this compound as a key intermediate to access a wide range of bioactive molecules and functionalized compounds with potential applications in drug discovery, materials science, and more.