16727-44-9

Basic information

• Product Name: 3,5-Dibromo-2,6-dimethoxypyridine, 99%
• Synonyms: 3,5-Dibromo-2,6-dimethoxypyridine, 99%
• CAS NO: 16727-44-9
• Molecular Formula: C₇H₇Br₂NO₂
• Molecular Weight: 296.96
• Mol File: 16727-44-9.mol

Chemical Properties

• Melting Point: 85-87°C
• Boiling Point: 261℃
• Flash Point: 112℃
• Appearance: /
• Density: 1.821
• Vapor Pressure: 0.0195mmHg at 25°C
• Refractive Index: 1.564
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 3,5-Dibromo-2,6-dimethoxypyridine, 99%(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dibromo-2,6-dimethoxypyridine, 99%(16727-44-9)
• EPA Substance Registry System: 3,5-Dibromo-2,6-dimethoxypyridine, 99%(16727-44-9)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-37
• Hazardous Substances Data: 16727-44-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3,5-Dibromo-2,6-dimethoxypyridine, 99% is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
3,5-Dibromo-2,6-dimethoxypyridine, 99% is used as a key intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its strong chemical properties make it suitable for creating effective and stable agrochemical products.
Used in Fine Chemicals Industry:
3,5-Dibromo-2,6-dimethoxypyridine, 99% is used as a starting material in the production of various fine chemicals, including specialty chemicals and intermediates for further chemical reactions. Its high purity and stable properties contribute to the quality and consistency of the final products.
Used in Chemical Research:
3,5-Dibromo-2,6-dimethoxypyridine, 99% is used as a research compound in various chemical studies. Its unique structure and properties make it an interesting subject for exploration in the fields of organic chemistry, medicinal chemistry, and materials science.

InChI:InChI=1/C7H7Br2NO2/c1-11-6-4(8)3-5(9)7(10-6)12-2/h3H,1-2H3

Upstream product

• 6231-18-1 2,6-dimethoxypyridine 

Downstream Products

• 1194315-79-1 3,5-dibromo-2,6-dimethoxy-4-diphenylphosphinopyridine 

Relevant articles and documents

Reinvestigation of the synthesis of 1-deazauridine

A thorough study for the synthesis of 1-deazauridine is described. 3-Bromo-2,6-dimethoxy-5-(-d-ribofuranosyl)pyridine, a synthetic precursor for 1-deazauridine, was prepared in seven steps from 2,6-dimethoxypyridine and d-ribose via the ribonolactone approach. Subsequent demethylation was unsuccessful but led to presumable anomerization and isomerization. The effort concluded that the synthesis of 1-deazauridine remained unachieved. Copyright Taylor and Francis Group, LLC.

Organic semiconductor photocatalyst can bifunctionalize arenes and heteroarenes

Photoexcited electron-hole pairs on a semiconductor surface can engage in redox reactions with two different substrates. Similar to conventional electrosynthesis, the primary redox intermediates afford only separate oxidized and reduced products or, more rarely, combine to one addition product. Here, we report that a stable organic semiconductor material, mesoporous graphitic carbon nitride (mpg-CN), can act as a visible-light photoredox catalyst to orchestrate oxidative and reductive interfacial electron transfers to two different substrates in a two- or three-component system for direct twofold carbon–hydrogen functionalization of arenes and heteroarenes. The mpg-CN catalyst tolerates reactive radicals and strong nucleophiles, is straightforwardly recoverable by simple centrifugation of reaction mixtures, and is reusable for at least four catalytic transformations with conserved activity.

The preparation of 2,6-disubstituted pyridinyl phosphine oxides as novel anti-cancer agents

A series of 2,6-dimethoxylpyridinyl phosphine oxides have been synthesized and examined for their antitumor activity. 2,6-Dimethoxy-3-phenyl-4-diphenylphosphinoylpyridine 2 has been employed as the lead compound for this study. We found out that the prese

A CONVENIENT SYNTHESIS OF AZAANTHRAQUINONES VIA POLAR ADDITION TO HETARYNE INTERMEDIATES. USE OF CARBANIONS DERIVED FROM 32-CYANO-1(3H)-ISOBENZOFURANONES

A convenient synthesis of 2-azaanthraquinones using the reaction of carbanions derived from 3-cyano-1(3H)-isobenzofuranones which serve as 1,4-dipole equivalents and hetaryne intermediates generated from bromopyridines and lithium diisopropylamide is reported.