857062-26-1

Basic information

• Product Name: tert-butyl-[6-chloro-2-(4-chloro-phenyl)-benzofuran-3-yloxy]-dimethyl-silane
• Synonyms: tert-butyl-[6-chloro-2-(4-chloro-phenyl)-benzofuran-3-yloxy]-dimethyl-silane
• CAS NO: 857062-26-1
• Molecular Weight: 393.385
• Mol File: 857062-26-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl-[6-chloro-2-(4-chloro-phenyl)-benzofuran-3-yloxy]-dimethyl-silane(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl-[6-chloro-2-(4-chloro-phenyl)-benzofuran-3-yloxy]-dimethyl-silane(857062-26-1)
• EPA Substance Registry System: tert-butyl-[6-chloro-2-(4-chloro-phenyl)-benzofuran-3-yloxy]-dimethyl-silane(857062-26-1)

Safety Data

• Hazardous Substances Data: 857062-26-1(Hazardous Substances Data)

Upstream product

• 857062-41-0 2-bromo-6-chloro-benzofuran-3-one 
• 3260-78-4 6-chlorobenzofuran-3(2H)-one 
• 1027376-65-3 (2-bromo-6-chloro-benzofuran-3-yloxy)-tert-butyl-dimethyl-silane 
• 1679-18-1 4-Chlorophenylboronic acid 

Downstream Products

• 1027538-72-2 6-chloro-2-(4-chloro-phenyl)-benzofuran-3-one 

Relevant articles and documents

A highly efficient synthesis of rocaglaols by a novel α-arylation of ketones

Rocaglaols are natural products exhibiting a range of biological activities. A new synthetic method for the α-arylation of ketones allows for the synthesis of previously inaccessible rocaglaol derivatives. The key sequence consists of a previously unreported Suzuki type reaction using brominated si-lyl enol ethers as substrates followed by deprotection of the arylated silyl enol ethers. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.