4,6-dibromoquinoline


Chemical Name: 4,6-dibromoquinoline
CAS Number: 927801-13-6
Product Number: AG0060TJ(AGN-PC-01LRBU)
Synonyms:
MDL No:
Molecular Formula: C9H5Br2N
Molecular Weight: 286.9507

Identification/Properties


Properties
BP:
352.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
286.954g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
286.877g/mol
Monoisotopic Mass:
284.879g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
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
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



4,6-Dibromoquinoline 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 in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. One key application of 4,6-Dibromoquinoline is in the synthesis of heterocyclic compounds. By reacting with different reagents and catalysts, it can undergo various transformations such as cyclization, halogenation, and cross-coupling reactions. This allows for the creation of complex molecular structures that are essential in drug discovery and development.Furthermore, 4,6-Dibromoquinoline is often used as a precursor in the preparation of fluorescent dyes and sensors. Its aromatic structure and bromine substituents facilitate functionalization reactions that enable the incorporation of specific properties for sensing and imaging applications. This makes it a valuable tool in the field of chemical biology and materials science.Additionally, the presence of bromine atoms in 4,6-Dibromoquinoline imparts unique reactivity that can be harnessed in transition metal-catalyzed coupling reactions. This enables the construction of carbon-carbon and carbon-heteroatom bonds, leading to the formation of diverse molecular architectures with potential biological activities.Overall, 4,6-Dibromoquinoline plays a crucial role in enabling the synthesis of intricate molecules with therapeutic and technological significance. Its versatility and reactivity make it a valuable asset in the toolbox of synthetic chemists exploring new frontiers in chemical research and development.