878209-81-5

Basic information

• Product Name: benzyl-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-p-tolyl-allyl]-amine
• Synonyms: benzyl-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-p-tolyl-allyl]-amine
• CAS NO: 878209-81-5
• Molecular Weight: 363.308
• Mol File: 878209-81-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-p-tolyl-allyl]-amine(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-p-tolyl-allyl]-amine(878209-81-5)
• EPA Substance Registry System: benzyl-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-p-tolyl-allyl]-amine(878209-81-5)

Safety Data

• Hazardous Substances Data: 878209-81-5(Hazardous Substances Data)

Upstream product

• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 865350-17-0 4,4,5,5-tetramethyl-2-(propa-1,2-dien-1-yl)-1,3,2-dioxaborolane 
• 624-31-7 4-tolyl iodide 
• 100-46-9 benzylamine 

Relevant articles and documents

Catalytic four-component assembly based on allenylboronate platform: New access to privileged allylic amine structures

We developed a novel palladium-catalyzed four-component assembly based on allenylboronate platform, by which privileged allylic amine structures can be constructed in a regioselective, stereoselective, and diversity-oriented manner. The boryl group acts not only as a useful group that can be transformed to various functional groups afterward but also as a stereochemical controller in the generation of key (π-allyl)palladium intermediates. A short synthesis of rolipram (selective phosphodiesterase-4 inhibitor) is also demonstrated. Copyright