851227-22-0

Upstream product

• 889361-58-4 1-(triisopropylsilyl)-1-[4-(triisopropylsilyloxymethyl)phenyl]ethyne 
• 13154-24-0 triisopropylsilyl chloride 
• 10602-04-7 (4-ethynylphenyl)methanol 
• 18282-51-4 4-iodo-benzyl alcohol 
• 863640-77-1 ((4-iodobenzyl)oxy)triisopropylsilane 
• 863640-78-2 1-triisopropylsilanyloxymethyl-4-trimethylsilanylethynyl-benzene 

Downstream Products

• 1429466-20-5 4-{2,5-dimethoxy-4-[2-(4-{2-[4-({[tris(propan-2-yl)silyl]oxy}methyl)phenyl]ethynyl}phenyl)ethynyl]phenyl}-2-methylbut-3-yn-2-ol 
• 1429466-21-6 {[4-(2-{4-[2-(4-ethynyl-2,5-dimethoxyphenyl)ethynyl]phenyl}ethynyl)phenyl]methoxy}triisopropylsilane 
• 1374643-32-9 C₂₆H₃₂OSi 
• 1374643-31-8 C₂₉H₃₈O₂Si 
• 851227-54-8 {4-[3-(4-azidomethylphenylethynyl)-5-isopropyl-4-methoxymethoxybenzyl]-3,5-dimethylphenoxy}acetic acid methyl ester 
• 863640-99-7 {4-[3-(4-hydroxymethyl-phenylethynyl)-5-isopropyl-4-methoxymethoxy-benzyl]-3,5-dimethyl-phenoxy}-acetic acid methyl ester 
• 863641-31-0 {4-[3-(4-azidomethyl-phenylethynyl)-4-hydroxy-5-isopropyl-benzyl]-3,5-dimethyl-phenoxy}-acetic acid methyl ester 
• 851227-35-5 (4-{3-isopropyl-4-methoxymethoxy-5-[4-(triisopropylsilanyloxymethyl)phenylethynyl]benzyl}-3,5-dimethylphenoxy)acetic acid methyl ester 

Relevant academic research and scientific papers

Synthesis, optical power limiting, and DFT calculations of triplet-triplet absorption of three novel Pt(II)-diacetylide chromophores

Three novel rod-like Pt(II)-diacetylides have been synthesized. When subjected to intense laser light, all three compounds showed strong optical power limiting at 532 and 600 nm. DFT calculated triplet-triplet electronic excitations were found to correlate with the nonlinear absorption.

Facile deprotection of bulky (trialkylsilyl)acetylenes with silver fluoride

An efficient and mild method is developed for the deprotection of bulky (trialkylsilyl)acetylenes. Treatment of 1-(triisopropylsilyl) acetylenes with silver fluoride, followed by hydrolysis of the intermediate silver acetylide with organic or inorganic ac

Hammett analysis of selective thyroid hormone receptor modulators reveals structural and electronic requirements for hormone antagonists

Selective thyroid hormone modulators that function as isoform-selective agonists or antagonists of the thyroid hormone receptors (TRs) might be therapeutically useful in diseases associated with aberrant hormone signaling. The most potent thyroid hormone