Boration [Synthetic Reagents] — includes diboron compounds and cyclic boronic ester derivatives that serve as sources of the boryl group in boration reactions. This category is classified as synthetic reagents for forming carbon-boron bonds and other non-halogen heteroatom bonds.
Reagents such as bis(pinacolato)diboron and bis(catecholato)diboron are widely used by synthetic organic chemists and organometallic chemists for transition-metal-catalyzed boration reactions, producing boronic esters that serve as coupling partners in Suzuki-Miyaura reactions. Other derivatives such as tetrahydroxydiboron and tetrakis(dimethylamino)diboron are used for C-H borylation or the formation of other organoboron compounds.
Product examples in this collection: TCI T3019 1630-79-1 Tetrakis(dimethylamino)diboron, TCI D4357 185990-03-8 2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, TCI T2953 13675-18-8 Tetrahydroxydiboron, TCI O0631 2247367-07-1 4,4,4',4',5,5,5',5'-Octaethyl-2,2'-bi(1,3,2-dioxaborolane), TCI B3757 13826-27-2 Bis(catecholato)diboron, TCI O0684 230299-46-4 4,4,4',4',6,6,6',6'-Octamethyl-2,2'-bi(1,3,2-dioxaborinane), TCI B2906 230299-21-5 Bis(hexylene Glycolato)diboron, TCI B1964 73183-34-3 Bis(pinacolato)diboron.
Pay attention to the type of protecting diol group on boronic esters (pinacol, catechol, neopentyl glycol, or hexylene glycol) because it affects the stability and reactivity of compounds in boration reactions. All products are genuine products of Tokyo Chemical Industry (TCI) Japan, with purity, packaging, and storage conditions listed on each item's page.
Other categories at the same level under C-X(Non-Halogen) Bond Formation [Synthetic Reagents], often used together in one laboratory workflow:
Back to C-X(Non-Halogen) Bond Formation [Synthetic Reagents]. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — official TCI Japan distributor in Indonesia — for availability checks and lead time directly from Japan.
