16688-89-4

Upstream product

• 102-25-0 1,3,5-triethylbenzene 
• 91-06-5 2-bromo-1,3,5-triethylbenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 50-00-0 formaldehyd 

Downstream Products

• 753460-15-0 5-(2,4,6-triethylphenyl)dipyrromethane 
• 1260113-89-0 1,3-bis(bromomethyl)-5-methyl-2,4,6-triethylbenzene 
• 1260113-91-4 1,3-bis(azidomethyl)-5-methyl-2,4,6-triethylbenzene 
• 1260113-68-5 1,3-bis(aminomethyl)-5-methyl-2,4,6-triethylbenzene 
• 1260113-66-3 C₂₅H₄₀N₄O₂ 
• 1260113-65-2 C₂₅H₄₄N₄ 
• 16358-57-9 1-methyl-2,4,6-triethylbenzene 
• 1228444-81-2 (S)-N-[2-(2,4,6-triethylbenzyl)aminophenyl]-S-isobutyl-S-phenylsulfoximine 
• 1055424-72-0 N-((2,4,6-trimethylphenyl)methylene)-N-oxide methanamine 
• 135779-06-5 1,3-diformyl-2,4,6-triethylbenzene 

Relevant academic research and scientific papers

Protecting the triplet excited state in sterically congested platinum porphyrin

Platinum tetrakis(2,4,6-triethylphenyl)porphyrin (Pt-1) was synthesized and its structural (X-ray), electrochemical and photophysical properties were fully characterized. Comparative studies of Pt-1 and its unsubstituted analog PtTPP show the effect of sterically congesting ortho-substituents on the dynamics of the triplet excited states. Lowered quenching rates by 3-4 times were observed for Pt-1vs. PtTPP in the presence of oxygen and perylene, and in concentration (self)-quenching experiments.

C3-symmetric proline-functionalized organocatalysts: Enantioselective michael addition reactions

C3-Symmetric, tripodal catalyst 4 based on 1,3,5- triethylbenzene, which incorporates the features of a molecular receptor, is shown to catalyze Michael addition reactions ofcarbonyl compounds to β-nitrostyrenes in a high stereoselectivity (up to 99:1a dr and up to 98%ee). Copyright