Indolines are aromatic bicyclic heterocycles consisting of a benzene ring fused to a five-membered nitrogen-containing ring. Indole alkaloids are extensively studied for their biological activities in several pharmaceutical areas, such as anticancer and antitumor. Among this chemical family, indolinone displays very promising antitumor properties by inhibiting various kinase families. These small molecules have a low molecular weight and most of them bind to protein kinases competing with ATP for the ATP-binding site. In addition to being building blocks in heterocyclic synthesis, indolines also have industrial applications as sensitizers in solar cells. The presence of a halogen allows these reagents to be used as substrates in various coupling reactions, including Suzuki-Miyaura cross-coupling reactions.

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CDS000133 6-Bromo-1H-indole-2,3-dione AldrichCPR C8H4BrNO2
CDS000344 6-Chloro-1H-indole-2,3-dione AldrichCPR C8H4ClNO2
734284 4-Bromoisoindoline hydrochloride 95% C8H8BrN · HCl
642371 5-Bromoindoline 97% C8H8BrN
CDS019338 5-Bromoisoindoline AldrichCPR C8H8BrN
CDS003126 5-Chloroindoline AldrichCPR C8H8ClN
CDS005250 5-Fluoro-2,3-dihydro-(1H)-indole AldrichCPR C8H8FN
CDS008960 6-Fluoro-2,3-dihydro-1H-indole AldrichCPR C8H8FN
CDS019734 5-Aminoindoline dihydrochloride AldrichCPR C8H12Cl2N2
CDS020494 1-Methyl-2-oxo-5-indolinesulfonyl chloride AldrichCPR C9H8ClNO3S
CBR00777 5-Methylindoline-2-carboxylic acid hydrochloride AldrichCPR C10H12ClNO2
CBR01137 2-(2,3-Dihydro-1H-indol-1-yl)ethanamine dihydrochloride AldrichCPR C10H16Cl2N2
161810 5-Chloro-2-methylene-1,3,3-trimethylindoline technical grade, 95% C12H14ClN
CDS010542 ciba blue 2b AldrichCPR C16H6Br4N2O2