1391092-44-6

Basic information

• Product Name: 3,5-di-tert-butyldimethylsilyloxybenzyl azide
• Synonyms: 3,5-di-tert-butyldimethylsilyloxybenzyl azide
• CAS NO: 1391092-44-6
• Molecular Weight: 393.677
• Mol File: 1391092-44-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,5-di-tert-butyldimethylsilyloxybenzyl azide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-di-tert-butyldimethylsilyloxybenzyl azide(1391092-44-6)
• EPA Substance Registry System: 3,5-di-tert-butyldimethylsilyloxybenzyl azide(1391092-44-6)

Safety Data

• Hazardous Substances Data: 1391092-44-6(Hazardous Substances Data)

Upstream product

• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 103929-83-5 methyl 3,5-bis(tert-butyldimethylsilyloxy)benzoate 
• 158139-69-6 5-(bromomethyl)-1,3-bis(tert-butyldimethylsilyloxy)-benzene 

Downstream Products

• 1391092-41-3 4-ferrocenyl-1-((3,5-dihydroxybenzyl)-1H-1,2,3-triazole) 
• 1391092-47-9 4-ferrocenyl-1-((3,5-bis-tert-butyldimethylsilyloxy)benzyl)-1H-1,2,3-triazole 

Relevant articles and documents

Synthesis, electrochemistry and anticancer activity of novel ferrocenyl phenols prepared via azide-alkyne 1,3-cycloaddition reaction

A series of monophenols and diphenols containing the ferrocene-C triazolyl and ferrocene-Ntriazolyl bond were prepared in a cycloaddition reaction of ethynylferrocene with aryl and benzyl azides and in a reaction of azidoferrocene with phenylacetylenes, respectively. The anticancer activity of the prepared compounds against hormone-dependent (MCF-7) and hormone-independent (HCC38) breast cancer cell lines was studied. The investigated compounds exhibited moderate anticancer activity against hormone-independent (IC50 ～ 15-48 μM) cancer cell line and low activity against hormone-dependent cancer cell line (IC50 ～ 84-98 μM).