594859-93-5

Basic information

• Product Name: 2,5-Pyrrolidinedione, 1-[[5-[2-[2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-4,5-dihydro-4, 4-dimethyl-3-furanyl]-2-methylpropoxy]-1-oxopentyl]oxy]-
• CAS NO: 594859-93-5
• Molecular Formula: C31H47NO7Si
• Molecular Weight: 573.802
• Mol File: 594859-93-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,5-Pyrrolidinedione, 1-[[5-[2-[2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-4,5-dihydro-4, 4-dimethyl-3-furanyl]-2-methylpropoxy]-1-oxopentyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Pyrrolidinedione, 1-[[5-[2-[2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-4,5-dihydro-4, 4-dimethyl-3-furanyl]-2-methylpropoxy]-1-oxopentyl]oxy]-(594859-93-5)
• EPA Substance Registry System: 2,5-Pyrrolidinedione, 1-[[5-[2-[2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-4,5-dihydro-4, 4-dimethyl-3-furanyl]-2-methylpropoxy]-1-oxopentyl]oxy]-(594859-93-5)

Safety Data

• Hazardous Substances Data: 594859-93-5(Hazardous Substances Data)

Upstream product

• 594859-92-4 5-(3-tert-butyldimethylsilyloxyphenyl)-4-(7-carboxy-1,1-dimethyl-3-oxaheptyl)-3,3-dimethyl-2,3-dihydrofuran 
• 74124-79-1 di(succinimido) carbonate 
• 594859-80-0 4-(7-carboxy-1,1-dimethyl-3-oxaheptyl )-5-(3-hydroxyphenyl)-3,3-dimethyl-2,3-dihydrofuran 
• 594859-79-7 4-(7-ethoxycarbonyl-1,1-dimethyl-3-oxaheptyl)-5-(3-methoxyphenyl)-3,3-dimethyl-2,3-dihydrofuran 

Downstream Products

• 949913-11-5 N-(4-(benzo[d]thiazol-2-yl)-3-methoxybenzyl)-5-(2-(2-(3-(tert-butyldimethylsilyloxy)phenyl)-4,4-dimethyl-4,5-dihydrofuran-3-yl)-2-methylpropoxy)pentanamide 

Relevant articles and documents

Synthesis of bicyclic dioxetanes tethering a fluororescer through an ω-carbamoyl-substituted linker and their high-performance chemiluminescence in an aqueous system

Bicyclic dioxetanes 3 and 4 tethering a fluorescein or 4-(benzothiazol-2- yl)-3-hydroxyphenyl moiety through a linker were synthesized by the use of dihydrofuran-intermediate 5 or its advanced intermediate 6. These dioxetanes underwent base-induced decomp