942063-15-2

Basic information

• Product Name: but-2-enoic acid 4-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]-1-methylhexyl ester
• Synonyms: but-2-enoic acid 4-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]-1-methylhexyl ester
• CAS NO: 942063-15-2
• Molecular Weight: 404.665
• Mol File: 942063-15-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: but-2-enoic acid 4-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]-1-methylhexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: but-2-enoic acid 4-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]-1-methylhexyl ester(942063-15-2)
• EPA Substance Registry System: but-2-enoic acid 4-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]-1-methylhexyl ester(942063-15-2)

Safety Data

• Hazardous Substances Data: 942063-15-2(Hazardous Substances Data)

Upstream product

• 271769-81-4 (1,1-dimethylethyl)[(2-iodophenyl)methoxy]dimethylsilane 
• 24395-10-6 (R)-hept-6-en-2-ol 
• 942063-14-1 7-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]heptan-2-ol 
• 623-68-7 trans-crotonic anhydride 

Downstream Products

• 942063-16-3 but-2-enoic acid 6-(2-hydroxymethylphenyl)-1-methylhexyl ester 
• 942063-17-4 but-2-enoic acid 6-(2-formylphenyl)-1-methylhexyl ester 

Relevant articles and documents

Application of the intramolecular yamamoto vinylogous aldol reaction to the synthesis of macrolides

An intramolecular version of the Yamamoto vinylogous aldol reaction, a method that employs the bulky Lewis acid ATPH to control the site of aldolization, is described. This macrocyclization process is effective for the construction of 10-, 12-, and 14-mem