1126479-87-5

Basic information

• Product Name: Benzoic acid, 4-cyano-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester
• Synonyms: Benzoic acid, 4-cyano-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester
• CAS NO: 1126479-87-5
• Molecular Formula: C16H20BNO4
• Molecular Weight: 301.15
• Mol File: 1126479-87-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-cyano-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-cyano-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester(1126479-87-5)
• EPA Substance Registry System: Benzoic acid, 4-cyano-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester(1126479-87-5)

Safety Data

• Hazardous Substances Data: 1126479-87-5(Hazardous Substances Data)

Upstream product

• 7153-22-2 ethyl 4-cyanobenzoate 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 269410-00-6 3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzoic acid ethyl ester 

Relevant articles and documents

Rhodium-catalyzed reductive decyanation of nitriles using hydrosilane as a reducing agent: Scope, mechanism and synthetic application

A rhodium-catalyzed reductive cleavage reaction of carbon-cyano bonds is developed using hydrosilane as a mild reducing agent. A wide range of nitriles, including aryl, benzyl, and p-hydrogen containing alkyl cyanides are applicable to this decyanation reaction. The method is also applicable to organic synthesis, in which benzyl cyanide is used as a benzyl anion equivalent and a cyano group functions as a removable ortho-directing group.