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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)-

5-Bromoimidazo[1,2-a]pyridine-2-carboxylic acid methyl ester

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Chemical Name: 5-Bromoimidazo[1,2-a]pyridine-2-carboxylic acid methyl ester
CAS Number: 1092351-65-9
Product Number: AG008U92(AGN-PC-0WAB8D)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


The 5-Bromoimidazo[1,2-a]pyridine-2-carboxylic acid methyl ester is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it suitable for forming key intermediates in the synthesis of diverse organic molecules. Additionally, its bromo functionality enables further derivatization through various coupling reactions, allowing for the introduction of additional functional groups to tailor the properties of the final product. In the field of medicinal chemistry, this compound finds applications in the development of novel drug candidates, where its structural features can be exploited to design molecules with specific biological activities. Its utility in chemical synthesis extends to the preparation of complex organic compounds with potential applications across different industries.