5329-89-5

Basic information

• Product Name: 1-(9,10-dihydrophenanthren-2-yl)ethanone
• CAS NO: 5329-89-5
• Molecular Formula: C₁₆H₁₄O
• Molecular Weight: 222.2818
• Mol File: 5329-89-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 392.1°C at 760 mmHg
• Flash Point: 173.2°C
• Density: 1.124g/cm³
• Vapor Pressure: 2.35E-06mmHg at 25°C
• Refractive Index: 1.609
• CAS DataBase Reference: 1-(9,10-dihydrophenanthren-2-yl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(9,10-dihydrophenanthren-2-yl)ethanone(5329-89-5)
• EPA Substance Registry System: 1-(9,10-dihydrophenanthren-2-yl)ethanone(5329-89-5)

Safety Data

• Hazardous Substances Data: 5329-89-5(Hazardous Substances Data)

Usage

General Description

1-(9,10-dihydrophenanthren-2-yl)ethanone, also known as 9,10-dihydroanthracen-2-yl methyl ketone, is an aromatic ketone compound with a chemical structure consisting of a phenanthrene ring system and a ketone functional group. It is a yellow crystalline solid with a strong odor, and it is sparingly soluble in water but soluble in organic solvents. 1-(9,10-dihydrophenanthren-2-yl)ethanone is primarily used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials. It has also been studied for its potential biological and pharmacological activities, such as its anti-inflammatory and antioxidant properties. Additionally, 1-(9,10-dihydrophenanthren-2-yl)ethanone is known to have potential industrial applications, particularly in the field of organic synthesis and chemical manufacturing.

Upstream product

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• 1175695-84-7 C₁₆H₁₄O 

Downstream Products

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

Relevant articles and documents

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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.

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.

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.