321735-69-7

Upstream product

• 321735-68-6 tris(4-bromo-2,3,5,6-tetramethylphenyl)borane 
• 95-93-2 1,2,4,5-tetramethylbenzene 
• 7553-56-2 iodine 
• 1646-54-4 1,4-dibromodurene 

Downstream Products

• 571187-32-1 B(C₆(CH₃)4I)(C₆(CH₃)4CCC₆H₄N(CH₃)2)2 
• 1046498-57-0 tris(4-(4-pyridyl)duryl)borane 
• 1335471-11-8 tris(2,3,5,6-tetramethyl-4-(pyridin-3-yl)phenyl)borane 
• 1048667-04-4 tris(2',3',5',6'-tetramethylbiphenyl-4-carboxylic acid)borane 
• 321735-72-2 tris(4-ethynyl-2,3,5,6-tetramethylphenyl)borane 
• 571187-33-2 4-(4-{bis-[4-(4-dimethylamino-phenylethynyl)-2,3,5,6-tetramethyl-phenyl]-boranyl}-2,3,5,6-tetramethyl-phenyl)-2-methyl-but-3-yn-2-ol 
• 571187-34-3 B(C₆(CH₃)4(CCH))(C₆(CH₃)4CCC₆H₄N(CH₃)2)2 
• 321735-70-0 tris[(trimethylsilylethynyl)duryl]borane 
• 1048667-03-3 tris(2',3',5',6'-tetramethylbiphenyl-4-methoxycarbonyl)borane 

Relevant academic research and scientific papers

Synthesis, structure and photoluminescence of two porous metal-organoboron frameworks with rtl topology

Rigid trigonal tris(3-pyridylduryl)borane L was synthesized through four steps in good overall yield from readily available 1,2,4,5-tetramethylbenzene and was used to construct two porous cadmium (II) complexes Cd(L)X 2?G (X = Cl, Br; G = guset

Chiral octupolar metal-organoboron NLO frameworks with (14,3) topology

(Chemical Equation Presented) Tunable NLO activity: The title compounds were efficiently assembled from the enantiopure and threefold-symmetric tris(4-pyridylduryl)borane ligand L through coordinative bonds. The Cd-organoboron framework (see picture) exhi

Tridurylboranes extended by three arylethynyl groups as a new family of boron-based π-electron systems

(equation presented) A series of tris(phenylethynylduryl)boranes (R-C6H4-C≡C-duryl)3B with various substituents R have been prepared as air-stable solids owing to the steric protection of the boron atom by the three bulky