1447933-44-9

Basic information

• Product Name: 2-(2-bromomethyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
• Synonyms: 2-(2-bromomethyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
• CAS NO: 1447933-44-9
• Molecular Weight: 327.026
• Mol File: 1447933-44-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(2-bromomethyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-bromomethyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(1447933-44-9)
• EPA Substance Registry System: 2-(2-bromomethyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(1447933-44-9)

Safety Data

• Hazardous Substances Data: 1447933-44-9(Hazardous Substances Data)

Upstream product

• 73183-34-3 bis(pinacol)diborane 
• 27060-75-9 4-bromo-3-methylanisole 

Downstream Products

• 377780-72-8 2-(2-(bromomethyl)phenyl)-4,4,5,5,-tetramethyl-1,3,2-dioxaborolane 
• 1447933-45-0 trimethyl-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-quaternaryammonium bromide 
• 1447933-51-8 C₁₁H₁₉BNO₃⁽¹⁺⁾*Br^(1-) 
• 25240-59-9 pinacolboronic acid 
• 1447933-55-2 (2-hydroxy-5-methoxybenzyl)trimethylquaternary ammonium bromide 
• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 1013914-85-6 2-(bromomethyl)-4-methoxyphenol 
• 11113-50-1 boric acid 
• 174671-92-2 1,3-dihydro-5-methoxy-1-hydroxy-2,1-benzoxaborole 
• 41951-76-2 2-hydroxy-5-methoxybenzyl alcohol 
• 495-08-9 gentisyl alcohol 
• 644-17-7 2-hydroxymethyl-1,4-benzoquinone 
• 195062-59-0 2-methylphenylboronic acid pinacol ester 
• 1447933-47-2 trimethyl-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-5-methoxybenzyl]-quaternaryammonium bromide 

Relevant articles and documents

Towards the enantioselective synthesis of axially chiral cyclic bis(bibenzyls) through sulfoxide-controlled diastereoselective Suzuki coupling

Natural macrocyclic bis(bibenzyls) exhibiting configurationally stable axially chiral biaryls are of high interest from a structural as well as from a synthetic point of view. An enantiopure sulfinyl auxiliary controlling an atropo-diastereoselective biar