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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)-

Benzenamine, 4-(5-isoxazolyl)-

Nc1ccc(cc1)c1ccno1 Request for Quotation
Chemical Name: Benzenamine, 4-(5-isoxazolyl)-
CAS Number: 832740-73-5
Product Number: AG0055X9(AGN-PC-019Y31)
Synonyms:
MDL No:
Molecular Formula: C9H8N2O
Molecular Weight: 160.1726

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid

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

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Chemical Structure


4-(Isoxazol-5-yl)aniline is a versatile compound commonly used in chemical synthesis for the development of various organic molecules. This compound serves as a valuable building block due to its unique structural features and reactivity, making it an essential component in the creation of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 4-(Isoxazol-5-yl)aniline acts as a key intermediate in the preparation of heterocyclic compounds. Its isoxazole ring and aniline moiety can undergo a variety of functional group transformations, such as halogenation, nitration, and acylation, to introduce specific chemical functionalities into the target molecules. This flexibility allows chemists to tailor the properties of the final products for specific applications.Additionally, the presence of both electron-rich and electron-deficient regions in 4-(Isoxazol-5-yl)aniline enables it to participate in diverse organic reactions, including nucleophilic aromatic substitutions, Suzuki couplings, and Heck reactions. These synthetic pathways provide access to a wide range of structurally complex and biologically active compounds for use in drug discovery and material science.Overall, the application of 4-(Isoxazol-5-yl)aniline in chemical synthesis offers chemists a powerful tool for the efficient construction of advanced molecular architectures with tailored properties and functionalities. Its versatility and reactivity make it an indispensable building block for the creation of innovative compounds in various fields of chemistry.