3-(2-chloro-5-methylpyrimidin-4-yl)-1H-indole|945016-62-6,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)-

3-(2-chloro-5-methylpyrimidin-4-yl)-1H-indole

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Chemical Name:	3-(2-chloro-5-methylpyrimidin-4-yl)-1H-indole
CAS Number:	945016-62-6
Product Number:	AG005WMG(AGN-PC-0C7HH0)
Synonyms:
MDL No:
Molecular Formula:	C13H10ClN3
Molecular Weight:	243.6916

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Chemical Structure

The compound 3-(2-Chloro-5-methylpyrimidin-4-yl)-1H-indole, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block for the creation of various organic compounds. With its unique structure combining an indole and pyrimidine ring system, $name$ offers a range of opportunities for the development of novel pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ can be utilized as a key intermediate in the production of biologically active molecules such as kinase inhibitors and potential anticancer agents. Its strategic positioning within a molecule allows for selective functionalization and modification to introduce specific chemical groups that may enhance the desired pharmacological properties.Furthermore, the presence of both electron-rich and electron-deficient moieties in the structure of $name$ enables it to engage in diverse chemical reactions, including cross-coupling reactions, heterocycle formation, and heteroatom substitutions. This versatility makes it a valuable component in the synthesis of complex organic molecules with tailored properties and functionalities.Overall, 3-(2-Chloro-5-methylpyrimidin-4-yl)-1H-indole emerges as a valuable tool in the hands of synthetic chemists, offering a wide array of possibilities for the construction of structurally diverse and biologically relevant compounds. Whether in the development of pharmaceuticals or the design of new materials, $name$ holds promise for driving innovation and discovery in the field of organic chemistry.