1. Home
  2. 5-(3-methylphenyl)-1,3-oxazole-4-carboxylic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

5-(3-methylphenyl)-1,3-oxazole-4-carboxylic acid

Cc1cccc(c1)c1ocnc1C(=O)O Request for Quotation
Chemical Name: 5-(3-methylphenyl)-1,3-oxazole-4-carboxylic acid
CAS Number: 914220-25-0
Product Number: AG00GUUG(AGN-PC-05IVIU)
Synonyms:
MDL No:
Molecular Formula: C11H9NO3
Molecular Weight: 203.19406

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-(m-Tolyl)oxazole-4-carboxylic acid is a versatile compound frequently employed in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and functional groups make it a valuable intermediate in the production of diverse molecular entities. The presence of an oxazole ring and a tolyl group enables this compound to participate in a range of organic reactions, including condensations, substitutions, and cyclizations, allowing for the generation of complex molecular frameworks. By serving as a starting material or a precursor, 5-(m-Tolyl)oxazole-4-carboxylic acid plays a crucial role in the synthesis of target molecules with specific biological activities or material properties. Its strategic position in the synthetic pathway of numerous compounds highlights its importance in modern chemical research and development.