6929-81-3

Basic information

• Product Name: 10-broMoanthracene-9-carboxylic acid
• Synonyms: 10-broMoanthracene-9-carboxylic acid;10-BROMO-9-ANTHRACENECARBOXYLIC ACID;(2Z,3E)-4-bromo-2,3-diethylidene-2,3-dihydronaphthalene-1-carboxylic acid
• CAS NO: 6929-81-3
• Molecular Formula: C₁₅H₉BrO₂
• Molecular Weight: 301.13476
• Mol File: 6929-81-3.mol
• Article Data: 7

Chemical Properties

• Melting Point: 273 °C
• Boiling Point: 513.9±23.0 °C(Predicted)
• Appearance: /
• Density: 1.615±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.37±0.30(Predicted)
• CAS DataBase Reference: 10-broMoanthracene-9-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 10-broMoanthracene-9-carboxylic acid(6929-81-3)
• EPA Substance Registry System: 10-broMoanthracene-9-carboxylic acid(6929-81-3)

Safety Data

• Hazardous Substances Data: 6929-81-3(Hazardous Substances Data)

Usage

General Description

10-Bromoanthracene-9-carboxylic acid is a chemical compound with the molecular formula C16H9BrO2. It is a derivative of anthracene, a polycyclic aromatic hydrocarbon, with a bromine atom substituted at the 10th position and a carboxylic acid group at the 9th position. 10-broMoanthracene-9-carboxylic acid is used in organic synthesis and chemical research as a building block for various organic molecules and materials. It is also studied for its potential biological and pharmaceutical applications. Its properties and reactivity make it useful for the development of new drugs, catalysts, and materials in the field of organic chemistry.

Upstream product

• 523-27-3 9,10-Dibromoanthracene 
• 124-38-9 carbon dioxide 
• 723-62-6 anthracen-9-carboxylic acid 
• 7726-95-6 bromine 

Downstream Products

• 1089318-91-1 ethyl 10-bromoanthracene-9-carboxylate 
• 1734-16-3 9-tert-butyl anthroate 

Relevant articles and documents

Synthesis and properties of ion-conducting poly(anthrylacetylene) derivatives

Poly(anthryacetylenes) bearing oligooxyethylene units were synthesized from 10-ethynyl-9-[3,6-dioxaheptyl]oxycarbonylanthracene (1) and 10-ethynyl-9-[3,6,9,12-tetraoxatridecyl]oxycarbonyl-anthracene (2) by using a transition metal catalyst, WCl6, in 30% and 34% yields, respectively. Both of the polymers were black solids and soluble in chloroform, tetrahydrofuran, acetone, etc., but insoluble in alcohols, aliphatic hydrocarbons, etc. The UV-vis spectra of the polymers showed absorption maxima and band edges at around 570 and 750 nm, respectively, indicating that the polymer chains possess highly extended conjugation. These polymers exhibited blue emission (emission maxima ≈470 nm) upon photoexcitation at 380 nm. Poly(2) showed a fairly large ionic conductivity (4.1 × 10-5 S/cm) at 80 °C upon doping with Li(CF3SO2)2N.

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