Trimethadione

(Isopropenyloxy)trimethylsilane is an enol silyl ether. It participates as nucleophile in Lewis acid-promoted C3-nucleophile substitution of tetracyclic bromide.

(Isopropenyloxy)trimethylsilane is an enol silyl ether. It participates as nucleophile in Lewis acid-promoted C3-nucleophile substitution of tetracyclic bromide.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 1,3,3-Trimethoxybutane may be used in chemical synthesis studies.

Mechanism of Diels-Alder reaction between 1-(trimethylsiloxy)-1,3-butadiene and 4,6-dinitrobenzofuroxan has been studied using state-of-the-art computational methods . Application 1-(Trimethylsiloxy)-1,3-butadiene is commonly employed as diene in

Mechanism of Diels-Alder reaction between 1-(trimethylsiloxy)-1,3-butadiene and 4,6-dinitrobenzofuroxan has been studied using state-of-the-art computational methods . Application 1-(Trimethylsiloxy)-1,3-butadiene is commonly employed as diene in

2&#8242,3&#8242,4&#8242-Trimethoxyacetophenone on reaction with BCl 3 gives the corresponding 2,3-dihydroxy-4-methoxy compounds .

2',4',5'-Trimethoxyacetophenone

2',4',6'-Trimethoxyacetophenone

2',4',6'-Trimethylacetophenone

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.