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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)-

Quinoline, 3-bromo-, 1-oxide

Brc1cc2ccccc2[n+](c1)[O-] Request for Quotation
Chemical Name: Quinoline, 3-bromo-, 1-oxide
CAS Number: 22615-00-5
Product Number: AG00BI1E(AGN-PC-0JWIF1)
Synonyms:
MDL No:
Molecular Formula: C9H6BrNO
Molecular Weight: 224.0540

Identification/Properties

Properties
Storage:
Room Temperature;Inert atmosphere;
Computed Properties
Molecular Weight:
224.057g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
222.963g/mol
Monoisotopic Mass:
222.963g/mol
Topological Polar Surface Area:
25.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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-Bromoquinoline 1-oxide is a versatile compound widely utilized in chemical synthesis as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and functional materials. This powerful reagent is particularly valuable in the synthesis of complex organic molecules due to its unique structure and reactivity.One key application of 3-Bromoquinoline 1-oxide is in the formation of heterocyclic compounds, which are essential components in drug development and material science. By serving as a precursor in the construction of heterocycles, this compound enables chemists to access a diverse range of chemical structures with potential biological activities.Moreover, 3-Bromoquinoline 1-oxide is a pivotal reagent in the synthesis of fluorescent dyes and probes. Its ability to undergo diverse chemical transformations allows for the facile incorporation of this compound into fluorescent molecules, which are crucial for imaging biological systems and studying complex biochemical processes.In addition, this compound plays a crucial role in the preparation of ligands for catalytic reactions. Its unique scaffold and functional groups provide a platform for the design and development of ligands that can enhance the efficiency and selectivity of various catalytic processes, opening up new avenues for sustainable chemical transformations.