Collection: C-Se Bond Formation [Synthetic Reagents]

C-Se Bond Formation [Synthetic Reagents] — contains organoselenium reagents such as diselenides and selenenyl halides used to form carbon–selenium bonds in organic synthesis. This class includes aliphatic and aromatic derivatives that act as electrophilic or nucleophilic sources of selenium groups.

C-Se Bond Formation [Synthetic Reagents] is used in electrophilic selenylation reactions of alkenes and enolates, the formation of organoselenium compounds for radical chemistry studies, and the synthesis of precursors for selenoxide elimination reactions. Organic chemists use reagents such as diphenyl diselenide and phenylselenenyl chloride for regioselective functionalization and as catalysts in certain oxidation reactions.

Example products in this collection: TCI P1322 34837-55-3 Phenylselenenyl Bromide, TCI D2186 1666-13-3 Diphenyl Diselenide, TCI P1091 5707-04-0 Phenylselenenyl Chloride, TCI D2717 1482-82-2 Dibenzyl Diselenide, TCI D4715 628-39-7 Diethyl Diselenide, TCI D3290 7101-31-7 Dimethyl Diselenide.

Consider the reagent form (diselenide versus selenenyl halide) according to the desired reaction mechanism, purity, and its sensitivity to moisture and oxidation during storage. All products are genuine products of Tokyo Chemical Industry (TCI) Japan, with purity, packaging, and storage conditions listed on each item's page.

Other parallel categories under Selenium Compounds [Non-Heterocyclic Building Blocks], often used together in one laboratory workflow:

Back to Selenium Compounds [Non-Heterocyclic Building Blocks]. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — the official distributor of TCI Japan in Indonesia — to check availability and lead time directly from Japan.

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