147496-14-8

Basic information

• Product Name: 6,6'-DIBROMO-[3,3']-BIPYRIDINE
• Synonyms: 6,6'-DIBROMO-[3,3']-BIPYRIDINE;6,6'-Dibromo-3,3'-bipyridine, tech. 90%
• CAS NO: 147496-14-8
• Molecular Formula: C₁₀H₆Br₂N₂
• Molecular Weight: 313.97604
• Mol File: 147496-14-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: ca 249℃
• Boiling Point: 411 °C at 760 mmHg
• Flash Point: 202.4 °C
• Appearance: /
• Density: 1.809g/cm³
• CAS DataBase Reference: 6,6'-DIBROMO-[3,3']-BIPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 6,6'-DIBROMO-[3,3']-BIPYRIDINE(147496-14-8)
• EPA Substance Registry System: 6,6'-DIBROMO-[3,3']-BIPYRIDINE(147496-14-8)

Safety Data

• Hazardous Substances Data: 147496-14-8(Hazardous Substances Data)

Usage

General Description

6,6'-Dibromo-[3,3']-bipyridine is a chemical compound with the formula C12H6N2Br2. It is a halogenated bipyridine derivative that is commonly used in coordination chemistry and organic synthesis. 6,6'-DIBROMO-[3,3']-BIPYRIDINE is known for its ability to form metal complexes, which are often employed as catalysts in various chemical reactions. Its unique structure and reactivity make it a valuable tool in the development of new materials and pharmaceuticals. Additionally, 6,6'-dibromo-[3,3']-bipyridine is a versatile building block for the preparation of organic molecules with diverse applications in the field of chemical research and development.

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Downstream Products

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Relevant articles and documents

Pd-catalyzed oxidative homocoupling of arylboronic acids in WEPA: A sustainable access to symmetrical biaryls under added base and ligand-free ambient conditions

Symmetrical and unsymmetrical biaryls comprises a diverse class of biologically eloquent organic compounds. We herein report, a quick and eco-friendly protocol for the synthesis of biaryls by an oxidative (aerobic) homocoupling of arylboronic acids (ABAs) using Pd(OAc)2 in water extract of pomogranate ash (WEPA) as an efficient agro-waste(bio)-derived aqueous (basic) media. The reactions were executed at ambient aerobic conditions in the absence of external base and ligand to result symmetrical biaryls in excellent yields. The use of renewable media with an effective exploitation of waste, short reaction times, excellent yields of products, easy separation of the products, unnecessating the external base, oxidant, ligand or volatile organic solvents and ambient reaction conditions are the vital insights of the present protocol.

Selbstorganisation von Multikomponentensystemen: spontane Bildung eines zylinderfoermigen Komplexes aus fuenf Liganden und sechs Metall-Ionen

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