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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)-

2-Oxazolepropanoicacid, 5-phenyl-

OC(=O)CCc1ncc(o1)c1ccccc1 Request for Quotation
Chemical Name: 2-Oxazolepropanoicacid, 5-phenyl-
CAS Number: 23485-68-9
Product Number: AG002NE0(AGN-PC-0KUSH7)
Synonyms:
MDL No:
Molecular Formula: C12H11NO3
Molecular Weight: 217.2206

Identification/Properties

Computed Properties
Molecular Weight:
217.224g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
217.074g/mol
Monoisotopic Mass:
217.074g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
238
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(5-Phenyloxazol-2-yl)propanoic acid is a versatile compound widely used in chemical synthesis. It serves as a key building block in the production of various pharmaceuticals, agrochemicals, and materials. Its unique structure containing an oxazole ring and a propionic acid moiety provides it with significant reactivity and functionality.In chemical synthesis, 3-(5-Phenyloxazol-2-yl)propanoic acid can be utilized as a precursor in the synthesis of complex molecules through various transformations. Its oxazole ring can undergo functionalization reactions, such as halogenation, alkylation, and acylation, to introduce additional substituents or structural modifications. The propionic acid group can also participate in esterification or amidation reactions to afford derivatives with altered physicochemical properties.Furthermore, the presence of the phenyl group in the molecule can impart specific properties to the final products, such as enhanced aromaticity, hydrophobicity, or biological activity. By incorporating 3-(5-Phenyloxazol-2-yl)propanoic acid into synthetic routes, chemists can access a diverse array of compounds with tailored structures and functionalities for various applications in the fields of medicine, agriculture, and materials science.