24415-36-9

Upstream product

• 128-39-2 2,6-di-tert-butylphenol 
• 10294-34-5 boron trichloride 

Downstream Products

• 1968-59-8 (2.4-(t-C₄H₉)2C₆H₃O)B(OH)2 
• 315238-61-0 (tert-butylamino)(2,6-tert-butylphenyloxy)(chloro)borane 
• 315238-67-6 (2,6-tert-butylphenyloxy)(chloro)(2,4,6-trimethylphenylamino)borane 
• 315238-70-1 (2,6-tert-butylphenyloxy)(chloro)(2,4,6-tri-tert-butylphenylamino)borane 
• 315238-65-4 (2,6-tert-butylphenyloxy)(chloro)(2,6-diisopropylphenylamino)borane 
• 315238-83-6 2,4-bis(2,6-di-tert-butylphenoxy)-1,3-bis(2,6-diisopropylphenyl)-1,3-diaza-2,4-diboretidine 
• 315238-85-8 2,4-bis(2,6-di-tert-butylphenoxy)-1,3-bis(2,4,6-trimethylphenyl)-1,3-diaza-2,4-diboretidine 
• 105916-58-3 N-(chloro(2,6-di-tert-butylphenoxy)boryl)-O-methyl-N-(trimethylsilyl)hydroxylamine 
• 315238-63-2 (2,6-di-tert-butylphenoxy)(chloro)(trimethylsilylamino)borane 

Relevant academic research and scientific papers

First B-organyloxy-substituted iminoboranes: preparation, stabilization, and reactivity

The amino(halo)(organyloxy)boranes ROB(X)N(H)R′ (R = 2,6-tBu2C6H3) X = Cl, R′ = tBu (7), SiMe3 (8), 2,6-iPr2C6H3 (9), 2,4,6-Me3C6H2 (10), 2,4,6-tBu3C6H2 (11); R = 2,6-C6H5)2C6H3, X = Cl, R′ = tBu (12); R = 2,6-tBu2C6H3) X = F, R′ = tBu (13), 2,6-iPr2C6H3 (14); R = tBu3C, X = F, R′ = iPr (15), tBu (16), SiMe3 (17)) were dehydrohalogenated with tert-butyllithium at low temperature.