7251-51-6

Basic information

• Product Name: 9,10-dimethylphenanthrene-9,10-diol
• Synonyms: 9,10-dimethylphenanthrene-9,10-diol
• CAS NO: 7251-51-6
• Molecular Formula: C16H16O2
• Molecular Weight: 240.297
• Mol File: 7251-51-6.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 394.9 °C at 760 mmHg
• Flash Point: 188.3 °C
• Appearance: /
• Density: 1.22 g/cm³
• Vapor Pressure: 6.05E-07mmHg at 25°C
• Refractive Index: 1.638
• CAS DataBase Reference: 9,10-dimethylphenanthrene-9,10-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-dimethylphenanthrene-9,10-diol(7251-51-6)
• EPA Substance Registry System: 9,10-dimethylphenanthrene-9,10-diol(7251-51-6)

Safety Data

• Hazardous Substances Data: 7251-51-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H16O2/c1-15(17)13-9-5-3-7-11(13)12-8-4-6-10-14(12)16(15,2)18/h3-10,17-18H,1-2H3

Upstream product

• 917-54-4 methyllithium 
• 84-11-7 9,10-phenanthrenequinone 
• 24017-95-6 2,2'-diacetylbiphenyl 
• 75-16-1 methylmagnesium bromide 
• 766-51-8 2-Chloroanisole 
• 7647-01-0 hydrogenchloride 
• 917-64-6 methyl magnesium iodide 
• 2733-80-4 10-hydroxy-10-methyl-9,10-dihydrophenanthren-9-one 
• 2142-68-9 1-(2-chlorophenyl)ethanone 
• 676-58-4 methylmagnesium chloride 

Downstream Products

• 73326-46-2 C₅₂H₄₂P₂⁽²⁺⁾*2Br^(1-) 
• 81650-56-8 7-methyl-5H-dibenzocyclohepten-5-one 
• 81568-57-2 phenanthrene-9,10-dicarboxylic acid 
• 24017-95-6 2,2'-diacetylbiphenyl 
• 57743-47-2 9,10-Bis(bromomethyl)phenanthrene 
• 73326-44-0 10-Methyl-9-brommethyl-phenanthren 

Relevant articles and documents

Organic electroluminescent compounds Organic electroluminescent material containing same and and organic electroluminescent device

The present disclosure relates to an organic electroluminescent compound, an organic electroluminescent material comprising the same, and an organic electroluminescent device. By comprising an organic electroluminescent compound according to the present d

Synthesis of linearly and angularly fused indane-based constrained α-amino acid derivatives

The benzocyclobutene-based α-amino acid derivative, ethyl 5-acetamido-2,4,5,6-tetrahydro-1H-cyclobuta[f]indene-5-carboxylate is synthesized via coupling of a benzocyclobutene-derived dibromide with ethyl isocyanoacetate as the key step, followed by hydrolysis and subsequent acetylation. This methodology is generalized in order to prepare various linearly and angularly fused indane-based α-amino acid derivatives. Georg Thieme Verlag Stuttgart - New York.

An efficient one-pot approach to phenanthrene derivatives using a catalyzed tandem Ullmann-pinacol coupling reaction

In the presence of catalyst (Ph3P)2NiCl2 and reductant Zn, the Ullmann reactions of ortho-halo aryl aldehydes generate biaryl-dialdehydes and zinc halides. Subsequently, ZnX2 can catalyze the intramolecular pinacol coupling reaction of biaryl-dialdehydes to form 9,10-dihydrophenanthrene-9,10-diols. One-pot synthesis of 9-phenanthrols can be achieved using this strategy.