imidazo[1,2-a]pyridin-2-ylmethanamine;dihydrochloride|452967-56-5,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

imidazo[1,2-a]pyridin-2-ylmethanamine;dihydrochloride

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Chemical Name:	imidazo[1,2-a]pyridin-2-ylmethanamine;dihydrochloride
CAS Number:	452967-56-5
Product Number:	AG00DJTJ(AGN-PC-0KKU2A)
Synonyms:
MDL No:
Molecular Formula:	C8H11Cl2N3
Molecular Weight:	220.0990

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Chemical Structure

Imidazo[1,2-a]pyridin-2-ylmethanamine dihydrochloride is a versatile compound extensively utilized in chemical synthesis as a key building block. This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials due to its unique structure and reactivity. Through its incorporation into synthetic pathways, Imidazo[1,2-a]pyridin-2-ylmethanamine dihydrochloride enables the efficient construction of complex molecular architectures with diverse applications in the field of organic chemistry. Its presence in a wide range of chemical reactions highlights its significance as a valuable tool for researchers and chemists seeking to access novel chemical entities and functional materials.