200481-96-5

Upstream product

• 100-52-7 benzaldehyde 
• 179061-63-3 C₂₇H₄₃NO₂Si 
• 179061-64-4 3-(N-tert-butyldimethylsiloxy-N-tert-butylamino)-5-tert-butylbenzophenone 
• 133817-83-1 N-(3-bromo-5-tert-butylphenyl)-N-(tert-butyldimethylsiloxy)-N-tert-butylamine 
• 179061-65-5 3-(N-tert-butyldimethylsiloxy-N-tert-butylamino)-5-tert-butylbenzophenone hydrazone 

Downstream Products

• 179061-66-6 [3-(N-ylooxy-tert-butylamino)-5-tert-butylphenyl]phenyldiazomethane 

Relevant academic research and scientific papers

Design and synthesis of diphenyldiazomethanes possessing stable aminoxyl radicals: Photolytic generation of quartet species and their reaction with C60

Diphenyldiazomethanes possessing stable tert-butylaminoxyl and Ullman's 'nitronyl nitroxide' radicals were prepared. The corresponding diphenylcarbenes substituted with the free radicals were generated by photolysis of the parent diazomethanes. From EPR f

Synthesis and EPR characterisation of [3-(N-ylooxy-tert-butylamino)-5-tert-butylphenyl]phenylcarbene with a quartet ground state

[3-(N-ylooxy-tert-butylamino)-5-tert-butylphenyl]-phenylcarbene, a potential new spin/magnetic coupling unit for extended spin systems, is designed, synthesized and found by EPR spectroscopy to have a quartet ground state.