262371-08-4

Upstream product

• 31732-31-7 1,1-dibutyl-1-stannacyclohexa-2,5-diene 
• 162608-99-3 {2,4,6-tris[bis(trimethylsilyl)methyl]phenyl}silane 

Downstream Products

• 1208329-28-5 C₆₄H₁₃₀Si₁₄ 
• 262371-11-9 1-chloro-1-{2,4,6-tris[bis(trimethylsilyl)methyl]phenyl}-1-silacyclohexa-2,4-diene 
• 262371-05-1 1-[2,4,6-Tris-(bis-trimethylsilanyl-methyl)-phenyl]-siline 
• 262371-10-8 1-hydroxy-1-{2,4,6-tris[bis(trimethylsilyl)methyl]phenyl}-1-silacylohexa-2,4-diene 

Relevant academic research and scientific papers

The chemistry of stable silabenzenes

Stable silabenzenes (1a; R = Tbt, 1b; R = Bbt) were synthesized by taking advantage of extremely bulky and efficient steric protection groups, 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl (Tbt) and 2,6-bis- [bis(trimethylsilyl)methyl]-4-[tris(trimethylsily

Synthesis and properties of an over-crowded Silabenzene stable at ambient temperature

Solid-state, room-temperature stability for silabenzene 1 is granted by the bulky silane rendering kinetic inertness. Silabenzene 1 is synthesized in good yield from the crowded chlorosilane 2 with tert-butyllithium. The delocalized, aromatic nature of 1