25308-63-8

Usage

Uses

Used in Scientific Research:
2-Phenanthrenecarboxylic acid methyl ester is used as a research compound for the synthesis of other complex chemical compounds. It serves as a building block in the development of new organic compounds with potential applications in various fields.
Used in Chemical Synthesis:
2-Phenanthrenecarboxylic acid methyl ester is used as a synthetic intermediate in the production of various organic compounds. Its unique structure and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Analytical Chemistry:
2-Phenanthrenecarboxylic acid methyl ester can be used as a reference compound or a standard in analytical chemistry. Its distinct properties and characteristics can be utilized for calibration of instruments and validation of analytical methods.
Used in Material Science:
2-Phenanthrenecarboxylic acid methyl ester may have potential applications in material science, particularly in the development of new polymers, coatings, or other materials with specific properties. Its aromatic structure and functional groups can contribute to the desired characteristics of these materials.

InChI:InChI=1/C16H12O2/c1-18-16(17)13-8-9-15-12(10-13)7-6-11-4-2-3-5-14(11)15/h2-10H,1H3

Upstream product

• 186581-53-3 diazomethane 
• 40452-20-8 phenanthrene-2-carboxylic acid 
• 85-01-8 phenanthrene 
• 5960-69-0 2-acetylphenanthrene 
• 5968-48-9 1-Phenanthren-1-yl-ethanone 
• 5329-89-5 2-acetyl-9,10-dihydrophenanthrene 
• 205823-24-1 methyl 2'-formyl-(1,1'-biphenyl)-4-carboxylate 
• 89005-09-4 1,3-dihydro-1-hydroxynaphtho<1,2-c>furan 
• 292638-85-8 acrylic acid methyl ester 
• 67-56-1 methanol 

Downstream Products

• 2606-54-4 2-phenanthrylmethanol 
• 104952-88-7 [1-Phenanthren-2-yl-meth-(E)-ylidene]-(4-tetradecyloxy-phenyl)-amine 
• 104931-69-3 (4-Dodecyloxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104984-85-2 (4-Decyloxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104931-68-2 (4-Nonyloxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104931-67-1 4-heptyloxy-N-(2-phenanthrylmethylene)aniline 
• 104931-66-0 (4-Heptyloxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104931-65-9 (4-Hexyloxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104952-87-6 (4-Pentyloxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104931-64-8 (4-Butoxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104931-63-7 [1-Phenanthren-2-yl-meth-(E)-ylidene]-(4-propoxy-phenyl)-amine 
• 104931-62-6 (4-Ethoxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 104931-61-5 (4-Methoxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 

Relevant academic research and scientific papers

A combined experimental and computational study on the cycloisomerization of 2-ethynylbiaryls catalyzed by dicationic arene ruthenium complexes

Ruthenium-catalyzed cycloisomerization of 2-ethynylbiaryls was investigated to identify an optimal ruthenium catalyst system. A combination of [η6-(p-cymene)RuCl2(PR3)] and two equivalents of AgPF6 effectively converted 2-ethynylbiphenyls into phenanthrenes in chlorobenzene at 120 °C over 20 h. Moreover, 2-ethynylheterobiaryls were found to be favorable substrates for this ruthenium catalysis, thus achieving the cycloisomerization of previously unused heterocyclic substrates. Moreover, several control experiments and DFT calculations of model complexes were performed to propose a plausible reaction mechanism.

1-Phenylisobenzofuran, 1-Phenylnaphthofuran, 1-Phenylnaphthofuran, and 3-Phenylnaphthofuran via Cyclic Hemiaminal, Hemiacetal, and Acetal Precursors

The title compounds have been generated via cyclic hemiaminal, hemiacetal, and acetal precursors and trapped in Diels-Alder reactions with several dienophiles.The precursors are easily prepared from o-bromobenzyl alcohol, 2-bromo-3-naphthalenemethanol, or

Properties of the Liquid Crystals formed by Certain 4-Alkoxy-N-(2-phenanthrylmethylene)anilines

The liquid crystal transition temperatures of twelve 4-alkoxy-N-(2-phenanthrylmethylene)anilines are reported and compared with those of corresponding members of similar homologous series of azomethines.Differences in liquid crytal thermal stability between comparable azomethines in which the -CH=N- linkage is reversed are discussed.