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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, 2-(4-bromophenyl)-, ethyl ester

CCOC(=O)c1coc(n1)c1ccc(cc1)Br Request for Quotation
Chemical Name: 4-Oxazolecarboxylic acid, 2-(4-bromophenyl)-, ethyl ester
CAS Number: 391248-23-0
Product Number: AG00I7Q3(AGN-PC-05W22G)
Synonyms:
MDL No:
Molecular Formula: C12H10BrNO3
Molecular Weight: 296.1167

Identification/Properties

Properties
BP:
380.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
296.12g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
294.984g/mol
Monoisotopic Mass:
294.984g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
267
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


Ethyl 2-(4-bromophenyl)oxazole-4-carboxylate is widely utilized in chemical synthesis as a versatile building block. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows for efficient functionalization and diversification, making it an essential component in the synthesis of complex organic molecules. With its strategic placement of the bromophenyl and oxazole moieties, Ethyl 2-(4-bromophenyl)oxazole-4-carboxylate offers synthetic chemists a valuable tool for creating novel compounds with specific biological activities or properties. Its broad applicability and compatibility with a range of reaction conditions make it a valuable resource for researchers seeking to develop innovative chemical solutions.