480434-20-6

Basic information

• Product Name: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine
• Synonyms: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine
• CAS NO: 480434-20-6
• Molecular Weight: 358.248
• Mol File: 480434-20-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine(480434-20-6)
• EPA Substance Registry System: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine(480434-20-6)

Safety Data

• Hazardous Substances Data: 480434-20-6(Hazardous Substances Data)

Upstream product

• 15862-19-8 5-bromo-2,2'-bipyridyl 
• 99770-93-1 benzene-1,4-diboronic acid bispinacol ester 
• 7732-18-5 water 
• 73183-34-3 bis(pinacol)diborane 
• 173960-45-7 5-(4-bromophenyl)-2,2'-bipyridine 
• 5467-74-3 4-Bromophenylboronic acid 

Downstream Products

• 1012323-27-1 9-benzyl-8-[4-(2,2'-bipyridine-5-yl)phenyl]adenine 
• 1130161-26-0 5-[4-(2,2'-bipyridin-5-yl)phenyl]-2'-deoxycytidine 
• 1130161-29-3 5-[4-(2,2'-bipyridin-5-yl)phenyl]-2'-deoxyuridine 

Relevant articles and documents

Guest encapsulation and self-assembly of a cavitand-based coordination capsule

The synthesis and spectroscopic characterization of a cavitand-based coordination capsule 1·4 BF4 of nanometer dimensions is described. Encapsulation studies of large aromatic guests as well as aliphatic guests were performed by using 1/s

Lewis Acid–Base Interaction-Controlled ortho-Selective C?H Borylation of Aryl Sulfides

An iridium/bipyridine-catalyzed ortho-selective C?H borylation of aryl sulfides was developed. High ortho-selectivity was achieved by a Lewis acid–base interaction between a boryl group of the ligand and a sulfur atom of the substrate. This is the first example of a catalytic and regioselective C?H transformation controlled by a Lewis acid–base interaction between a ligand and a substrate. The C?H borylation reaction could be conducted on a gram scale, and with a bioactive molecule as a substrate, demonstrating its applicability to late-stage regioselective C?H borylation. A bioactive molecule was synthesized from an ortho-borylated product by converting the boryl and methylthio groups of the product.

Fullerene sensors based on calix[5]arene

A new class of fullerene sensors based on calix[5]arenes has produced the highly sensitive detection of C60 and C70.