1421598-63-1

Basic information

• Product Name: C₂₆H₃₈O₃Si
• Synonyms: C₂₆H₃₈O₃Si
• CAS NO: 1421598-63-1
• Molecular Weight: 426.671
• Mol File: 1421598-63-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₆H₃₈O₃Si(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₆H₃₈O₃Si(1421598-63-1)
• EPA Substance Registry System: C₂₆H₃₈O₃Si(1421598-63-1)

Safety Data

• Hazardous Substances Data: 1421598-63-1(Hazardous Substances Data)

Upstream product

• 147974-20-7 3-[4-(tert-butyl-dimethyl-silanyloxy)phenyl]propionaldehyde 
• 183140-16-1 C₁₇H₂₆O₃Si 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 622397-33-5 (S)-1-(4-((tert-butyldimethylsilyl)oxy)phenyl)hex-5-en-3-ol 
• 123-08-0 4-hydroxy-benzaldehyde 
• 522602-18-2 ethyl 3-(4-((tert-butyl(dimethyl)silyl)oxy)phenyl)propanoate 
• 120743-99-9 p-[(tert-butyldimethylsilyl)oxy]benzaldehyde 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 1303501-13-4 1,9-bis(4-hydroxyphenyl)-3,7-dihydroxynonan-5-one 
• 1421598-67-5 (+)-(3S,7S)-1,9-bis(4-(tert-butyldimethylsilyloxy)phenyl)-3,7-dihydroxynonan-5-one 
• 1421598-64-2 C₂₆H₃₈O₄Si 
• 1421598-65-3 C₄₁H₆₂O₆Si₂ 

Relevant articles and documents

Enantioselective total synthesis of (-)-ericanone

The first total synthesis of (-)-ericanone was achieved in 10 steps with a 16% overall yield from p-hydroxybenzaldehyde. Notable features of this stereocontrolled approach include a Keck allylation to install the stereocenter at C3 and a 1,5-anti aldol reaction to install the hydroxyl group at C7.