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Organoborates

Organoborates are convenient nucleophilic reagents due to their stability towards air and moisture; however, the stability does not hamper their high reactivity in a large variety of reactions, such as oxidative cross-coupling between the alkynyl and aryl ligands of the borates, forming an sp-sp2 carbon-carbon bond. Organoborates are involved in the sequence hydroboration-oxidation and are being investigated as electrolytes for lithium batteries.

Product #

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Description

Molecular Formula

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92330 Trimethyl borate purum, ≥99.0% (GC) C3H9BO3
447218 Trimethyl borate 99.999% (trace metal basis) C3H9BO3
443999 Trimethyl borate purified by redistillation, ≥99.5% C3H9BO3
452920 Trimethyl borate ≥98% C3H9BO3
790877 Tris(2,2,2-trifluoroethyl) borate 97% C6H6BF9O3
T59307 Triethyl borate 99% C6H15BO3
673943 2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 96% C7H15BO3
417149 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 98% C9H19BO3
197335 Triisopropyl borate ≥98% C9H21BO3
348635 Tris(trimethylsilyl) borate 99% C9H27BO3Si3
236608 Tri-tert-butyl borate 98% C12H27BO3
90795 Tributyl borate ≥99.0% (T) C12H27BO3
418714 Triphenyl borate ≥97% C18H15BO3
CDS000471 Trihexadecyl borate AldrichCPR C48H99BO3