1192037-24-3

Basic information

• Product Name: 2,6-Dibromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
• Synonyms: 2,6-Dibromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine;2,6-Dibromopyridine-4-boronic acid pinacol ester;(2,6-DIBROMOPYRIDIN-4-YL)BORONIC ACID PINACOL ESTER
• CAS NO: 1192037-24-3
• Molecular Formula: C₁₁H₁₄BBr₂NO₂
• Molecular Weight: 362.85336
• Product Categories: Organic boronic acid
• Mol File: 1192037-24-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,6-Dibromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dibromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(1192037-24-3)
• EPA Substance Registry System: 2,6-Dibromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(1192037-24-3)

Safety Data

• Hazardous Substances Data: 1192037-24-3(Hazardous Substances Data)

Usage

General Description

2,6-Dibromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound with the molecular formula C12H14BBr2NOS. It is a complex and highly specific organic compound used in various chemical and pharmaceutical applications. 2,6-Dibromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is primarily utilized in the synthesis of advanced organic materials and as a reagent in organic synthesis. It is also used in the production of pharmaceutical drugs and as a building block in the creation of more complex chemical structures. Additionally, this compound has shown potential as a valuable tool in the development of new materials and drug discovery research. Its unique structure and properties make it a valuable and versatile compound in the field of organic chemistry.

Upstream product

• 626-05-1 2,6-Dibromopyridine 
• 73183-34-3 bis(pinacol)diborane 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Downstream Products

• 220616-68-2 (1H)-2,6-dibromo-4-pyridone 

Relevant articles and documents

Stabilized Gallylene in a Pincer-Type Ligand: Synthesis, Structure, and Reactivity of PGaIP-Ir Complexes

Iridium complexes having a pincer-type gallylene ligand were successfully synthesized utilizing bis(phosphino)terpyridine as an efficient scaffold for the Ir?GaI bond. The stabilization of the gallylene moiety by the pincer-type structure enabled various reactions at Ir with keeping the gallylene ligand intact, leading to unique structures and reactivities of PGaIP?Ir complexes.

Microwave-assisted, Ir-catalyzed aromatic C-H borylation

One-step conversions of 1,3-disubstituted benzenes to aryl boronates and 2,6-disubstituted pyridines to heteroaryl boronates are described. Microwave heating was used for all reactions. [(COD)Ir(μ-OMe)]2 and 4,4′-di-tert-butyl-2,2′-bipyridine w