96710-97-3

Basic information

• Product Name: 9,9'-oxybis(9-phenyl-9H-fluorene)
• Synonyms: 9,9'-oxybis(9-phenyl-9H-fluorene)
• CAS NO: 96710-97-3
• Molecular Weight: 498.624
• Mol File: 96710-97-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 9,9'-oxybis(9-phenyl-9H-fluorene)(CAS DataBase Reference)
• NIST Chemistry Reference: 9,9'-oxybis(9-phenyl-9H-fluorene)(96710-97-3)
• EPA Substance Registry System: 9,9'-oxybis(9-phenyl-9H-fluorene)(96710-97-3)

Safety Data

• Hazardous Substances Data: 96710-97-3(Hazardous Substances Data)

Upstream product

• 101884-29-1 nitric acid-(9-phenyl-fluoren-9-yl ester) 
• 25022-99-5 9-chloro-9-phenyl-9H-fluorene 
• 25603-67-2 9-phenyl-fluoren-9-ol 

Downstream Products

• 78388-22-4 ethyl-(9-phenyl-fluoren-9-yl)-ether 
• 25603-67-2 9-phenyl-fluoren-9-ol 

Relevant articles and documents

Deoxygenation of tertiary and secondary alcohols with sodium borohydride, trimethylsilyl chloride, and potassium iodide in acetonitrile

The deoxygenation of tertiary and secondary alcohols to give the corresponding alkanes is conventionally performed using an organosilane and a strong acid. In this study, a deoxygenation method was developed for tertiary and secondary alcohols, using trimethylsilane and trimethylsilyl iodide generated in situ from sodium borohydride and trimethylsilyl chloride, and trimethylsilyl chloride and potassium iodide, respectively. With our method, tertiary and secondary alcohols, which provided stable carbocations, were converted into the corresponding alkanes. This paper also presents the optimization of the reaction conditions, the reaction mechanism, as well as the scope and limitations of the method.