1196156-59-8

Basic information

• Product Name: 2,6-Dibromo-4-chloropyridine
• Synonyms: 2,6-Dibromo-4-chloropyridine
• CAS NO: 1196156-59-8
• Molecular Formula: C5H2Br2ClN
• Molecular Weight: 271.33708
• Mol File: 1196156-59-8.mol

Chemical Properties

• Boiling Point: 276.5±35.0 °C(Predicted)
• Appearance: /
• Density: 2.136±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: -2.93±0.10(Predicted)
• CAS DataBase Reference: 2,6-Dibromo-4-chloropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dibromo-4-chloropyridine(1196156-59-8)
• EPA Substance Registry System: 2,6-Dibromo-4-chloropyridine(1196156-59-8)

Safety Data

• Hazardous Substances Data: 1196156-59-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2,6-Dibromo-4-chloropyridine is utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique structure and strong halogenation properties contribute to the development of new drugs with improved therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-Dibromo-4-chloropyridine serves as a crucial building block for the creation of novel agrochemicals. Its incorporation into these compounds can enhance their effectiveness in pest control and crop protection.
Used in Fine Chemicals Industry:
2,6-Dibromo-4-chloropyridine is employed as a reagent in the synthesis of fine chemicals. Its versatility in chemical reactions allows for the production of a wide range of specialty chemicals used in various applications.
Used in Materials Science:
2,6-Dibromo-4-chloropyridine has been studied for its potential applications in materials science. The unique properties of 2,6-Dibromo-4-chloropyridine may contribute to the development of new materials with specific characteristics for use in various industries.
Used as a Precursor in Chemical Compound Development:
2,6-Dibromo-4-chloropyridine also acts as a precursor in the development of new chemical compounds. Its strong halogenation properties and reactivity in chemical reactions make it an essential component in the synthesis of innovative and advanced chemicals.

Upstream product

• 626-05-1 2,6-Dibromopyridine 

Downstream Products

• 133785-60-1 2,6-diphenyl-4-chloro pyridine 
• 856852-60-3 2,6-dibromo-4-phenoxypyridine 

Relevant articles and documents

NITROGEN-CONTAINING AROMATIC COMPOUNDS AND METAL COMPLEXES

To provide nitrogen-containing aromatic compounds with excellent oxygen reduction activity, metal complexes containing them, and catalysts and electrodes employing the same, the present invention provides an aromatic compound satisfying the following conditions (a) and (b): (a) It has 2 or more structures surrounded by at least 4 coordinatable nitrogen atoms (which structures may be the same or different), (b) At least one of the nitrogen atoms composing the structure is a nitrogen atom in a 6-membered nitrogen-containing heterocyclic ring.

Continuous process for the production of polybromopyridine compounds

A continuous process for producing a polybromopyridine compound comprises admixing a polychloropyridine compound with an anhydrous water soluble solvent in a first reaction zone to form a solution of the polychloropyridine compound. Hydrogen bromide gas is introduced into the solution while maintaining the temperature in the range of from about 70° to about 140° C. to produce a solution of the polybromopyridine compound. The solution is cooled to a temperature in the range of from about 5° to about 35° C. to precipitate the polybromopyridine compound from the anhydrous solvent. The polybromopyridine compound is separated from the anhydrous solvent and the anhydrous solvent is returned to the first reaction zone. Polybromopyridine compounds of increased purity are produced in a process having reduced material, energy and operating costs. The process does not require the use of water or other co-solvents nor the distillation of the reaction product mixture.