714964-20-2

Upstream product

• 50-00-0 formaldehyd 
• 526197-85-3 4-tert-butyl-5-[3-(cyanomethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 866129-66-0 5-(3-bromophenyl)-4-tert-butyl-3,3-dimethyl-2,3-dihydrofuran 
• 866129-69-3 4-tert-butyl-5-(3-formylphenyl)-3,3-dimethyl-2,3-dihydrofuran 
• 866129-75-1 5-[3-(bromomethyl)phenyl]-4-tert-butyl-3,3-dimethyl-2,3-dihydrofuran 
• 866129-72-8 4-tert-butyl-5-[3-(hydroxymethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 

Downstream Products

• 714964-21-3 5-tert-butyl-1-[3-(1-cyanoethenyl)phenyl]-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane 
• 866129-88-6 4-tert-butyl-5-{3-[1-cyano-3,3-bis(methoxycarbonyl)butyl]phenyl}-3,3-dimethyl-2,3-dihydrofuran 
• 866130-03-2 4-tert-butyl-5-[3-(3-cyano-4,5-dihydro-5,5-diphenyl-3H-pyrazol-3-yl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 866129-89-7 5-tert-butyl-1-{3-[1-cyano-3,3-bis(methoxycarbonyl)butyl]phenyl}-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane 

Relevant academic research and scientific papers

Intramolecular charge-transfer-induced chemiluminescent decomposition of 1,2-dioxetanes bearing a phenylmethanide anion

Dioxetanes (1) bearing a phenyl moiety substituted with a methylène or methine having an electron-withdrawing group(s) (-CH2-Ew or -CH(X)-Ew) and dioxetane (2) bearing a 3-(l-cyanoethenyl)phenyl group were synthesized. Treatment of dioxetanes (