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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)-

5-Isoxazolamine, 3-(4-bromophenyl)-

Brc1ccc(cc1)c1noc(c1)N Request for Quotation
Chemical Name: 5-Isoxazolamine, 3-(4-bromophenyl)-
CAS Number: 119162-53-7
Product Number: AG000I9W(AGN-PC-0LOEYT)
Synonyms:
MDL No: MFCD06199354
Molecular Formula: C9H7BrN2O
Molecular Weight: 239.0687

Identification/Properties

Computed Properties
Molecular Weight:
239.072g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
237.974g/mol
Monoisotopic Mass:
237.974g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
171
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(4-Bromophenyl)isoxazol-5-amine is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals. Its ability to react selectively at the isoxazole ring and bromophenyl group makes it an ideal candidate for constructing complex structures with precise control over functional group placement. Chemists leverage the reactivity of 3-(4-Bromophenyl)isoxazol-5-amine in coupling reactions, substitution reactions, and heterocycle syntheses to achieve tailored molecular architectures in drug development, materials science, and agrochemical research. Its potential applications extend to the synthesis of biologically active compounds, advanced materials, and intermediates for organic transformations, highlighting its significance in the realm of chemical synthesis.