25315-06-4

Usage

Uses

Used in Pharmaceutical Industry:
1,5-Dibromo-2,6-dimethoxynaphthalene is used as an intermediate in the production of pharmaceuticals for its ability to contribute to the synthesis of various medicinal compounds. Its unique structure allows it to be a key component in the development of drugs with specific therapeutic properties.
Used in Organic Synthesis:
In the realm of organic synthesis, 1,5-Dibromo-2,6-dimethoxynaphthalene is utilized as a valuable intermediate. Its chemical properties make it suitable for use in the creation of a wide range of organic compounds, expanding the scope of chemical research and development.
Used in Research Applications:
1,5-Dibromo-2,6-dimethoxynaphthalene is also employed in research settings, where it serves as a fundamental building block for the exploration and creation of new biologically active molecules. Its versatility in chemical reactions and potential to form complex structures make it an essential tool for scientific inquiry.
Safety Precautions:
Given the potential hazards associated with 1,5-Dibromo-2,6-dimethoxynaphthalene, it is crucial to handle this chemical with care. It may be harmful if ingested, inhaled, or comes into contact with skin or eyes. Therefore, it is imperative to adhere to proper safety precautions and handling procedures to mitigate any risks associated with its use.

InChI:InChI=1/C12H10Br2O2/c1-15-9-5-3-8-7(11(9)13)4-6-10(16-2)12(8)14/h3-6H,1-2H3

Upstream product

• 5486-55-5 2,6-dimethoxylnaphthalene 
• 581-43-1 2.6-dihydroxynaphthalene 
• 132178-78-0 1,5-dibromo-2,6-dihydroxynaphthalene 
• 77-78-1 dimethyl sulfate 

Relevant academic research and scientific papers

On-surface Synthesis of a Chiral Graphene Nanoribbon with Mixed Edge Structure

Chiral graphene nanoribbons represent an important class of graphene nanomaterials with varying combinations of armchair and zigzag edges conferring them unique structure-dependent electronic properties. Here, we describe the on-surface synthesis of an un

Intermolecular Palladium(0)-Catalyzed Atropo-enantioselective C-H Arylation of Heteroarenes

Atropisomeric (hetero)biaryls are motifs with increasing significance in ligands, natural products, and biologically active molecules. The straightforward construction of the stereogenic axis by efficient C-H functionalization methods is extremely rare an

A novel methoxy-decorated metal-organic framework exhibiting high acetylene and carbon dioxide storage capacities

A methoxy-decorated novel metal-organic framework (MOF), Cu2(DTPD) (ZJU-12, H4DTPD = 5,5′-(2,6-dimethoxynaphthalene-1,5-diyl)diisophthalic acid) with optimized pore space and open metal sites, was solvothermally synthesized and structurally characterized. The activated ZJU-12a displays a moderately high BET (Brunauer-Emmett-Teller) surface area of 2316 m2 g?1. Due to the pore size of the crystal being consistent with the molecular size and kinetic diameters of C2H2 and CO2, ZJU-12a exhibits a high C2H2 storage capacity of 244 cm3 g?1 and CO2 capture capacity of 134 cm3 g?1 at room temperature.

A New Microporous Metal-Organic Framework for Highly Selective C2H2/CH4 and C2H2/CO2 Separation at Room Temperature

We have successfully designed and synthesized a new tetracarboxylic linker, which constructed its first three-dimensional microporous metal-organic framework (MOF), [Cu2(DDPD)(H2O)2]?Gx (ZJU-13, H4DDPD=5,5'-(2,6-dihydroxynaphthalene-1,5-diyl)diisophthalic acid, ZJU=Zhejiang University, G = guest molecules) via solvothermal reaction. Due to open Cu2+ sites and optimized pore size, the activated ZJU-13a displays high separation selectivity for C2H2/CH4 of 74 and C2H2/CO2 of 12.5 at low pressure by using Ideal Adsorbed Solution Theory (IAST) simulation at room temperature.