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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)-

Phenol, 4-(2-benzoxazolyl)-

Oc1ccc(cc1)c1nc2c(o1)cccc2 Request for Quotation
Chemical Name: Phenol, 4-(2-benzoxazolyl)-
CAS Number: 3315-19-3
Product Number: AG00CNFG(AGN-PC-0O8ZSB)
Synonyms:
MDL No:
Molecular Formula: C13H9NO2
Molecular Weight: 211.2161

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Benzo[d]oxazol-2-yl)phenol, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the preparation of various functionalized molecules and pharmaceutical intermediates.One of the key applications of 4-(Benzo[d]oxazol-2-yl)phenol is in the synthesis of novel heterocyclic compounds. By utilizing this compound as a starting material, chemists can access a diverse array of oxazole derivatives through efficient synthetic routes. These oxazole derivatives exhibit promising biological activities and structural motifs, making them valuable targets for drug discovery and development.Additionally, 4-(Benzo[d]oxazol-2-yl)phenol can be employed in the construction of organic frameworks with tunable electronic properties. Its aromatic nature and oxazole moiety allow for the incorporation of this compound into conjugated systems, leading to the formation of materials with tailored optical and electronic characteristics. This feature is particularly advantageous in the fabrication of organic electronic devices and fluorescent probes.Furthermore, the ability of 4-(Benzo[d]oxazol-2-yl)phenol to undergo diverse chemical transformations, such as substitution reactions and functional group manipulations, enhances its utility in synthetic chemistry. By leveraging the reactivity of this compound, researchers can access a wide range of structurally diverse compounds with potential applications in various fields, including materials science and medicinal chemistry.