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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)-

6-bromo-3-iodoimidazo[1,2-a]pyrazine

Brc1ncc2n(c1)c(I)cn2 Request for Quotation
Chemical Name: 6-bromo-3-iodoimidazo[1,2-a]pyrazine
CAS Number: 1245644-42-1
Product Number: AG000M8R(AGN-PC-0BHSE0)
Synonyms:
MDL No:
Molecular Formula: C6H3BrIN3
Molecular Weight: 323.9166

Identification/Properties

Computed Properties
Molecular Weight:
323.919g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
322.856g/mol
Monoisotopic Mass:
322.856g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
157
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-Bromo-3-iodoimidazo[1,2-a]pyrazine is a versatile compound widely utilized in chemical synthesis for its unique reactivity and structural features. In organic chemistry, it serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials due to its ability to participate in diverse chemical reactions. This heterocyclic compound exhibits exceptional compatibility with a range of coupling reactions, such as Suzuki-Miyaura cross-coupling, Sonogashira coupling, and Heck reaction, enabling the efficient construction of complex molecules. Furthermore, the bromine and iodine substituents on the imidazo[1,2-a]pyrazine scaffold offer strategic handle for further derivatization, facilitating the development of novel compounds with enhanced properties. Its utility extends to the synthesis of bioactive compounds, advanced materials, and molecular probes, highlighting its significance in modern chemical research and development.