174362-59-5

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 69-72-7 salicylic acid 

Downstream Products

• 69-72-7 salicylic acid 
• 827575-54-2 2-(tert-butyldimethylsilanyloxy)-benzoyl chloride 
• 525-82-6 FLAVONE 
• 41255-30-5 4'-methylflavone 
• 223511-25-9 1-(2-((tert-butyldimethylsilyl)oxy)phenyl)-4-methoxybut-2-yn-1-one 
• 223511-29-3 1-[2-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-hydroxy-4-methyl-pent-2-yn-1-one 
• 223511-23-7 1-[2-(tert-butyl-dimethyl-silanyloxy)-phenyl]-6-chloro-hex-2-yn-1-one 
• 223511-19-1 1-[2-(tert-butyldimethylsilyloxy)phenyl]-3-phenylprop-2-yn-1-one 
• 223511-27-1 1-[2-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4,4-diethoxy-but-2-yn-1-one 
• 223511-21-5 1-[2-(tert-butyl-dimethyl-silanyloxy)-phenyl]-3-p-tolyl-propynone 
• 223511-31-7 1-[2-(tert-butyl-dimethyl-silanyloxy)-phenyl]-3-cyclohex-1-enyl-propynone 

Relevant academic research and scientific papers

The chemoselective and efficient deprotection of silyl ethers using trimethylsilyl bromide

An efficient and chemoselective cleavage of silyl ethers (primary, secondary and aromatic) by using catalytic quantities of trimethylsilyl bromide (TMSBr) in methanol is reported. A wide range of alkyl silyl ethers such as TBS, TIPS, and TBDPS can be chemoselectively cleaved in high yield in the presence of aryl silyl ethers. The deprotection of silyl esters was also achieved employing catalytic quantities of TMSBr. The Royal Society of Chemistry 2008.