5329-89-5

Usage

Uses

Used in Pharmaceutical Industry:
1-(9,10-dihydrophenanthren-2-yl)ethanone is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and properties, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(9,10-dihydrophenanthren-2-yl)ethanone is utilized as a component in the synthesis of different agrochemicals, potentially enhancing crop protection and yield.
Used in Material Science:
1-(9,10-dihydrophenanthren-2-yl)ethanone is employed as a precursor in the creation of novel materials, leveraging its chemical properties to engineer advanced material solutions.
Used in Organic Synthesis:
As a key intermediate in organic synthesis, 1-(9,10-dihydrophenanthren-2-yl)ethanone is used to construct a wide array of organic compounds, serving as a versatile component in chemical reactions.
Used in Chemical Manufacturing:
In the field of chemical manufacturing, 1-(9,10-dihydrophenanthren-2-yl)ethanone is applied in the production process of various chemicals, playing a crucial role in the synthesis of specialty and fine chemicals.
Used in Biological and Pharmacological Research:
1-(9,10-dihydrophenanthren-2-yl)ethanone is studied for its potential biological and pharmacological activities, such as anti-inflammatory and antioxidant properties, which may lead to its use in therapeutic applications.

Upstream product

• 776-35-2 9,10-dihydrophenanthrene 
• 75-36-5 acetyl chloride 
• 75-15-0 carbon disulfide 
• 7446-70-0 aluminium trichloride 
• 79-03-8 propionyl chloride 
• 98-88-4 benzoyl chloride 
• 98-95-3 nitrobenzene 
• 79-30-1 isobutyryl chloride 
• 79-04-9 chloroacetyl chloride 
• 1175695-84-7 C₁₆H₁₄O 

Downstream Products

• 64057-62-1 9,10-dihydrophenanthrene-2-carboxylic acid 
• 25308-63-8 methyl phenanthrene-2-carboxylate 
• 40452-20-8 phenanthrene-2-carboxylic acid 
• 90145-96-3 4-tetradecyloxy-N-(9,10-dihydro-2-phenanthrylmethylene)aniline 
• 89988-22-7 trans-9,10-dihydro-2-styrylphenanthrene 
• 89988-20-5 9,10-dihydro-2-<(triphenylphosphonio)methyl>phenanthrene bromide 
• 89988-21-6 cis-9,10-dihydro-2-styrylphenanthrene 
• 89988-17-0 1-<2-(9,10-dihydro-2-phenanthryl)-2-oxoethyl>pyridinium iodide 
• 5960-69-0 2-acetylphenanthrene 

Relevant academic research and scientific papers

LYSOPHOSPHATIDIC ACID RECEPTOR ANTAGONISTS

Compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or diagnose diseases, disorders, or conditions associated with one or more of the lysophosphatidic acid receptors are provided.

Multiscale charge injection and transport properties in self-assembled monolayers of biphenyl thiols with varying torsion angles

This article describes the molecular structure-function relationship for a series of biphenylthiol derivatives with varying torsional degree of freedom in their molecular backbone when self-assembled on gold electrodes. These biphenylthiol molecules chemisorbed on Au exhibit different tilt angles with respect to the surface normal and different packing densities. The charge transport through the biphenylthiol self-assembled monolayers (SAMs) showed a characteristic decay trend with the effective monolayer thickness. Based on parallel pathways model the tunneling decay factor β was estimated to be 0.27 A-1. The hole mobility of poly(3-hexylthiophene)-based thin-film transistors incorporating a biphenylthiol SAM coating the Au source and drain electrodes revealed a dependence on the injection barrier with the highest occupied molecular orbital (HOMO) level of the semiconductor. The possible role of the resistivity of the SAMs on transistor electrodes on the threshold voltage shift is discussed. The control over the chemical structure, electronic properties, and packing order of the SAMs provides a versatile platform to regulate the charge injection in organic electronic devices. Controlled charge injection! Biphenylthiols with different substituents between phenyl groups in the bridge position, once chemisorbed onto gold source-drain electrodes, can be used to vary the charge injection and electrical performances of organic thin-film transistors. By varying the torsion angle between the phenyl rings, one can introduce changes in packing densities and tilt angles of the molecules self-assembled on the electrode that play a direct role in influencing the charge transport through the molecular monolayer (see figure). Copyright

Diene-yne cyclisation reactions of 1-ethynyl-2-vinyl-3,4- dihydronaphthalenes and 1-ethynyl-2-vinylnaphthalenes

The reaction of 1-ethynyl-2-vinyl-3,4-dihydronaphthalenes and 1-ethynyl-2-vinylnaphthalenes over RuCI2(p-cymene) PPh3 leads to 9,10-dihydrophenanthrenes and phenanthrenes in those cases where the ethynyl group in the substrates carries a terminal proton. When 1-phenylethynyl-2-vinyl-3,4-dihydronaphthalenes or 1-phenylethynyl-2- vinylnaphthalenes are reacted over Pt(PPh3)4, 1-methylene-1H-benz[e]-4,5-dihydroindenes and 1-methylene-1H-benz[e]indenes are formed.

ANTI-ANDROGEN COMPOUNDS

Disclosed are novel classes of anti-androgen including dihydrophenanthrene derivatives, their method of synthesis and their use in treating disorders associated with excessive androgenic activities.

RECHERCHES SUR LES SUBSTANCES MESOGENES-VIII; PREPARATION ET PROPERTIES MESOMORPHES DE SERIES ISOMETRIQUES

The synthesis and the mesomorphic properties of various series of isometric mesogenic compounds are described.It is confirmed that isometric mesogenic molecules may be nematogenic and/or smectogenic according to the position of the polar rigid core.