203583-94-2

Upstream product

• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 10323-39-4 4-bromo-2-tert-butylphenol 
• 261903-05-3 3-tert-Butyl-2-(methoxymethoxy)phenol 
• 261903-04-2 1-(tert-butyl)-2-(methoxymethoxy)benzene 
• 4026-05-5 3-tert-butylbenzene-1,2-diol 
• 88-18-6 2-tert-Butylphenol 
• 76-09-5 2,3-dimethyl-2,3-butane diol 

Downstream Products

• 1309777-06-7 C₂₇H₄₀N₂O₆ 
• 1309781-34-7 C₂₇H₃₇N₂O₆ 

Relevant academic research and scientific papers

Rules for Magnetic Exchange in Azulene-Bridged Biradicals: Quo Vadis?

Electronic coupling through organic bridges facilitates magnetic exchange interactions and controls electron transfer and single-molecule device electron transport. Electronic coupling through alternant π-systems (e.g., benzene) is better understood than

Nitronyl nitroxide radicals as organic memory elements with both n- and p-type properties

Can't fight the SEEPR: Simultaneous electrochemical electron paramagnetic resonance reveals that a molecule containing the nitronyl nitroxide (NN) radical (structure and red layer) is redox-active, with switchability between oxidized and reduced states. An organic NN radical device utilizes the dual p- and n-type properties in a memory device. Copyright