865087-46-3

Upstream product

• 361543-99-9 4-methoxy-2,6-dimethylphenylboronic acid 
• 70564-92-0 4-bromo-3,5-dimethyl-pyridine 1-oxide 
• 865087-44-1 4-(4-methoxy-2,6-dimethylphenyl)-3,5-dimethyl-pyridin-1-ol 
• 6267-34-1 2-bromo-5-methoxy-1,3-dimethyl-benzene 
• 7463-51-6 4-bromo-3,5-dimethylphenol 

Downstream Products

• 865087-56-5 4-(4-iodo-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine 
• 865087-49-6 4-(3,5-dimethylpyridin-4-yl)-3,5-dimethyl-phenylamine 
• 865087-48-5 4-(3,5-dimethylpyridin-4-yl)-N-(diphenylmethylene)-3,5-dimethyl-benzenamine 
• 865087-47-4 2,6-di-tert-butyl-4-{2-[4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenyl]-vinyl}phenol 
• 865087-54-3 trifluoromethane sulfonic acid 4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenyl ester 

Relevant academic research and scientific papers

Ultralarge hyperpolarizability twisted π-electron system electro-optic chromophores: Synthesis, solid-state and solution-phase structural characteristics, electronic structures, linear and nonlinear optical properties, and computational studies

This contribution details the synthesis and chemical/physical characterization of a series of unconventional twisted π-electron system electro-optic (EO) chromophores. Crystallographic analysis of these chromophores reveals large ring-ring dihedral twist

Efficient synthesis and structural characteristics of zwitterionic twisted π-electron system biaryls

(Chemical Equation Presented) A series of unconventional twisted π-electron system molecules has been synthesized via Suzuki cross-coupling of two sterically hindered arenes. Crystallographic analysis of these molecules reveals a large ring-ring dihedral