Imidazo[1,2-a]pyrazin-8-amine, 6-bromo-


Chemical Name: Imidazo[1,2-a]pyrazin-8-amine, 6-bromo-
CAS Number: 117718-84-0
Product Number: AG007QTO(AGN-PC-0KP2HQ)
Synonyms:
MDL No: MFCD00874115
Molecular Formula: C6H5BrN4
Molecular Weight: 213.0347

Identification/Properties


Computed Properties
Molecular Weight:
213.038g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
211.97g/mol
Monoisotopic Mass:
211.97g/mol
Topological Polar Surface Area:
56.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
154
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#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



6-Bromoimidazo[1,2-a]pyrazin-8-amine, also known as $name$, is a valuable chemical intermediate widely utilized in organic synthesis. Its unique structure and functional groups make it an important building block for the creation of diverse compounds in the field of medicinal chemistry, pharmaceuticals, and materials science.In chemical synthesis, 6-Bromoimidazo[1,2-a]pyrazin-8-amine serves as a key starting material for the generation of various heterocyclic compounds due to its reactivity and versatility. It acts as a nucleophilic substrate in cross-coupling reactions, specifically in Suzuki-Miyaura and Heck couplings, leading to the formation of complex molecular structures. Additionally, its ability to undergo substitution and functionalization reactions enables the synthesis of novel derivatives with enhanced biological activities or tailored physicochemical properties.Furthermore, the presence of the bromine moiety in 6-Bromoimidazo[1,2-a]pyrazin-8-amine offers opportunities for further transformations such as palladium-catalyzed coupling reactions, halogen exchange reactions, and transition metal-catalyzed cross-couplings, allowing for the introduction of diverse functional groups and modifications.Overall, the strategic incorporation of 6-Bromoimidazo[1,2-a]pyrazin-8-amine in chemical synthesis facilitates the access to structurally diverse compounds with potential applications in drug discovery, agrochemicals, and materials development. Its utility as a versatile intermediate highlights its significance in advancing the field of organic chemistry and contributing to the creation of innovative molecules with valuable properties.