127666-66-4

Upstream product

• 17100-59-3 (4-bromo-2,6-dimethylphenyl)methanol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 5757-66-4 4-bromo-2,6-dimethylbenzonitrile 
• 5769-33-5 2,6-dimethyl-4-bromobenzaldehyde 

Downstream Products

• 127666-67-5 3-[4-(tert-Butyl-dimethyl-silanyloxymethyl)-3,5-dimethyl-phenyl]-3-trifluoromethyl-diaziridine 
• 127666-68-6 2,6-dimethyl-4<(trifluoromethyl)diazirinyl>benzyl alcohol 
• 127666-74-4 2,6-Dimethyl-4-(3-trifluoromethyl-3H-diazirin-3-yl)-benzaldehyde 
• 127666-75-5 3-[4-(tert-Butyl-dimethyl-silanyloxymethyl)-3,5-dimethyl-phenyl]-3-trifluoromethyl-3H-diazirine 
• 127685-64-7 (2E,4E,6E,8E)-9-[2,6-Dimethyl-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-3,7-dimethyl-nona-2,4,6,8-tetraenal 
• 127666-69-7 (2E,4E,6E,8E)-9-[2,6-Dimethyl-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-3,7-dimethyl-nona-2,4,6,8-tetraenoic acid ethyl ester 
• 127666-70-0 C₂₁H₂₀⁽³⁾HF₃N₂O 
• 127666-70-0 C₂₁H₂₀⁽³⁾HF₃N₂O 
• 127666-70-0 C₂₁H₂₀⁽³⁾HF₃N₂O 

Relevant academic research and scientific papers

N-Heterocyclic Olefins as Electron Donors in Combination with Triarylborane Acceptors: Synthesis, Optical and Electronic Properties of D–π–A Compounds

N-heterocyclic olefins (NHOs), relatives of N-heterocyclic carbenes (NHCs), exhibit high nucleophilicity and soft Lewis basic character. To investigate their π-electron donating ability, NHOs were attached to triarylborane π-acceptors (A) giving donor (D)