91394-96-6

Basic information

• Product Name: 2,6-DIBROMO-1,5-DIMETHOXYNAPHTHALENE
• Synonyms: 2,6-DIBROMO-1,5-DIMETHOXYNAPHTHALENE
• CAS NO: 91394-96-6
• Molecular Formula: C₁₂H₁₀Br₂O₂
• Molecular Weight: 346.01
• Mol File: 91394-96-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 403.1 °C at 760 mmHg
• Flash Point: 166.2 °C
• Appearance: /
• Density: 1.696 g/cm³
• Vapor Pressure: 2.43E-06mmHg at 25°C
• Refractive Index: 1.633
• CAS DataBase Reference: 2,6-DIBROMO-1,5-DIMETHOXYNAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIBROMO-1,5-DIMETHOXYNAPHTHALENE(91394-96-6)
• EPA Substance Registry System: 2,6-DIBROMO-1,5-DIMETHOXYNAPHTHALENE(91394-96-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 91394-96-6(Hazardous Substances Data)

Usage

General Description

The chemical 2,6-Dibromo-1,5-dimethoxynaphthalene is a synthetic organic compound with the molecular formula C12H10Br2O2. It is a derivative of naphthalene and contains two bromine atoms and two methoxy groups. 2,6-Dibromo-1,5-dimethoxynaphthalene is used in chemical research and organic synthesis as a building block for various molecules and materials. It has potential applications in the pharmaceutical industry, as well as in the development of new materials and compounds for industrial and research purposes. 2,6-Dibromo-1,5-dimethoxynaphthalene is known for its unique chemical properties and structural features, making it a valuable tool in the field of organic chemistry.

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

Upstream product

• 84-59-3 2,6-dibromo-1,5-naphthalenediol 
• 77-78-1 dimethyl sulfate 
• 158380-97-3 2,6-dibromo-5-methoxy-[1]naphthol 
• 10075-63-5 1,5-dimethoxynaphthalene 
• 7726-95-6 bromine 
• 71-43-2 benzene 
• 83-56-7 1,5-dihydroxynaphthalene 
• 74-88-4 methyl iodide 

Relevant articles and documents

Butterfly Effects Arising from Starting Materials in Fused-Ring Electron Acceptors

We designed and synthesized a series of fused-ring electron acceptors (FREAs) based on naphthalene-fused octacyclic cores end-capped by 3-(1,1-dicyanomethylene)-5,6-difluoro-1- indanone (NOICs) using a bottom-up approach. The NOIC series shares the same end groups and side chains, as well as similar fused-ring cores. The butterfly effects, arising from different methoxy positions in the starting materials, impact the design of the final FREAs, as well as their molecular packing, optical and electronic properties, charge transport, film morphology, and performance of organic solar cells. The binary-blend devices based on this NOIC series show power conversion efficiencies varying from 7.15% to 14.1%, due to the different intrinsic properties of the NOIC series, morphologies of blend films, and voltage losses of devices.

Tuning the size of macrocyclic cavities in trianglimine macrocycles

The synthesis of aromatic dicarboxaldehydes is described along with their reactivity in the [3 + 3] cyclocondensation reaction with (1R,2A)- diaminocyclohexane to give trianglimine macrocycles. In particular, the scope and limitation of the reaction with regard to complete control of the cavity size of the macrocycles is discussed producing a total of 11 macrocycles with different cavity sizes ranging from 9 to 23 A. The Royal Society of Chemistry 2005.