347840-57-7

Basic information

• Product Name: 2-bromo-3-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-dimethoxy-6-(3-methyl-but-2-enyl)-cyclohexa-2,5-dienone
• Synonyms: 2-bromo-3-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-dimethoxy-6-(3-methyl-but-2-enyl)-cyclohexa-2,5-dienone
• CAS NO: 347840-57-7
• Molecular Weight: 569.611
• Mol File: 347840-57-7.mol

Chemical Properties

• CAS DataBase Reference: 2-bromo-3-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-dimethoxy-6-(3-methyl-but-2-enyl)-cyclohexa-2,5-dienone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-3-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-dimethoxy-6-(3-methyl-but-2-enyl)-cyclohexa-2,5-dienone(347840-57-7)
• EPA Substance Registry System: 2-bromo-3-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-dimethoxy-6-(3-methyl-but-2-enyl)-cyclohexa-2,5-dienone(347840-57-7)

Safety Data

• Hazardous Substances Data: 347840-57-7(Hazardous Substances Data)

Upstream product

• 347840-66-8 [[2-bromo-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-6-methoxyphenyl]methoxy](1,1-dimethylethyl)diphenylsilane 
• 347840-56-6 [2-bromo-6-methoxy-3-(3-methyl-but-2-enyloxy)-benzyloxy]-tert-butyl-diphenyl-silane 
• 347840-54-4 2-bromo-3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-4-methoxyphenol 
• 347840-65-7 2-bromo-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-6-methoxybenzene-methanol 
• 347840-53-3 2-bromo-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-6-methoxybenzaldehyde 
• 347840-64-6 2-bromo-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-6-hydroxybenzaldehyde 
• 1194-98-5 2,5-Dihydroxybenzaldehyde 
• 67-56-1 methanol 
• 347840-55-5 2-bromo-3-(tert-butyl-diphenyl-silanyloxymethyl)-4-methoxy-6-(3-methyl-but-2-enyl)-phenol 
• 241127-72-0 2-bromo-3,6-dihydroxy-benzaldehyde 

Downstream Products

• 347840-59-9 C₃₃H₄₁BrO₅Si 
• 347840-61-3 C₃₆H₄₆O₅Si 
• 347840-58-8 (2S,4S)-8-Bromo-7-(tert-butyl-diphenyl-silanyloxymethyl)-2,4-dimethyl-10-(3-methyl-but-2-enyl)-1,5-dioxa-spiro[5.5]undeca-7,10-dien-9-one 

Relevant articles and documents

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(matrix presented) Enantioselective syntheses of the potent antifungal agent (-)-jesterone, its hydroxy epimer, and a dimeric quinone epoxide derivative are reported. The synthesis involves diastereoselective epoxidation of a chiral quinone monoketal deri