6-bromo-7-chloroquinoxaline


Chemical Name: 6-bromo-7-chloroquinoxaline
CAS Number: 1210047-58-7
Product Number: AG00HFUN(AGN-PC-0CTVTP)
Synonyms:
MDL No:
Molecular Formula: C8H4BrClN2
Molecular Weight: 243.4878

Identification/Properties


Computed Properties
Molecular Weight:
243.488g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
241.925g/mol
Monoisotopic Mass:
241.925g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



6-Bromo-7-chloroquinoxaline is a valuable chemical intermediate widely used in chemical synthesis. It plays a crucial role in organic chemistry as a versatile building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique structure and reactivity, this compound is frequently employed in the creation of complex organic molecules through diverse synthetic pathways.In chemical synthesis, 6-Bromo-7-chloroquinoxaline serves as a key starting material for the development of new drugs, such as antiviral and antibacterial agents. Its functional groups enable selective modifications and functionalizations, making it a valuable tool for medicinal chemists aiming to design potent bioactive compounds. Additionally, this compound can be utilized in the synthesis of specialty chemicals, dyes, and materials with specific properties.Moreover, 6-Bromo-7-chloroquinoxaline has demonstrated utility in the preparation of heterocyclic compounds with diverse biological activities. By incorporating this intermediate into various synthetic routes, chemists can access a wide range of novel molecules with potential therapeutic benefits. Its compatibility with different reaction conditions and its ability to participate in various chemical transformations make it a sought-after component in the arsenal of synthetic chemists worldwide.