25543-68-4

Basic information

• Product Name: 1,5-DIHYDROXYNAPHTHALENE-2,6-DICARBOXYLIC ACID
• Synonyms: 1,5-DIHYDROXYNAPHTHALENE-2,6-DICARBOXYLIC ACID;5-Dihydroxynaphthalene-2,6-dicarboxylic acid
• CAS NO: 25543-68-4
• Molecular Formula: C₁₂H₈O₆
• Molecular Weight: 248.19
• Mol File: 25543-68-4.mol

Chemical Properties

• Boiling Point: 503.2°C at 760 mmHg
• Flash Point: 272.2°C
• Appearance: /
• Density: 1.706g/cm³
• Vapor Pressure: 6.01E-11mmHg at 25°C
• Refractive Index: 1.791
• CAS DataBase Reference: 1,5-DIHYDROXYNAPHTHALENE-2,6-DICARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-DIHYDROXYNAPHTHALENE-2,6-DICARBOXYLIC ACID(25543-68-4)
• EPA Substance Registry System: 1,5-DIHYDROXYNAPHTHALENE-2,6-DICARBOXYLIC ACID(25543-68-4)

Safety Data

• Hazardous Substances Data: 25543-68-4(Hazardous Substances Data)

Usage

Uses

Used in Electrostatographic Developer Toner Industry:
1,5-DIHYDROXYNAPHTHALENE-2,6-DICARBOXYLIC ACID is used as a charge-controlling agent for enhancing the performance of electrostatographic developer toner. Its chemical structure allows it to effectively control the charge properties of the toner particles, leading to improved print quality and reduced issues related to toner aggregation or dispersion.

InChI:InChI=1/C12H8O6/c13-9-5-1-3-7(11(15)16)10(14)6(5)2-4-8(9)12(17)18/h1-4,13-14H,(H,15,16)(H,17,18)

Upstream product

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Downstream Products

• 688316-48-5 di[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl] 1,5-di[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]naphthalene-2,6-dicarboxylate 
• 605-89-0 1,5-diacetoxynaphthalene 

Relevant articles and documents

NAPHTHALENE BASED LITHIUM COMPOUNDS, A PROCESS FOR THEIR PREPARATION, THEIR USE AS SOLID ORGANIC CATALYST, AND THEIR USE IN RECHARGEABLE NON-AQUEOUS LITHIUM-AIR BATTERY CELLS

The present invention relates to novel naphthalene-based compounds, to their process of preparation, and to their use as Solid Organic Catalysts (SOC) in lithium-air battery cells to promote oxygen reactions. The invention also concerns a lithium-air battery cell wherein the positive electrode comprises a SOC according to the invention, as well as a battery pack comprising several lithium-air battery cells according to the invention. The use of a battery pack according to the invention as a rechargeable battery for vehicles, such as electric vehicles and hybrid vehicles, electronic devices, and stationary power generating devices, is also part of the invention. Finally, the invention is directed at a vehicle, an electronic device, and a stationary power generating device, comprising a battery pack according to the invention.

Asymmetric synthesis of ternaphthalenes via an ester-mediated nucleophilic aromatic substitution reaction

A convenient method is presented for the asymmetric synthesis of axially chiral 1,1′:5′,1″- and 1,1′:4′,1″- ternaphthalenes via the ester-mediated nucleophilic aromatic substitution reaction. Thus, treatment of dimenthyl 1,5-dimenthoxynaphthalene-2,6- dic