605-87-8

Basic information

• Product Name: 3-HYDROXY-PHENANTHRENE
• Synonyms: 3-HYDROXY-PHENANTHRENE;3-Phenanthrenol;3-Phenanthrol;NSC 30984
• CAS NO: 605-87-8
• Molecular Formula: C₁₄H₁₀O
• Molecular Weight: 194.23
• Product Categories: Various Metabolites and Impurities;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Aromatics
• Mol File: 605-87-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 92-94°C
• Boiling Point: 404.5 °C at 760 mmHg
• Flash Point: 197.7 °C
• Appearance: Tan Solid
• Density: 1.244 g/cm³
• Vapor Pressure: 4.02E-07mmHg at 25°C
• Refractive Index: 1.753
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
• PKA: 9.57±0.30(Predicted)
• CAS DataBase Reference: 3-HYDROXY-PHENANTHRENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-HYDROXY-PHENANTHRENE(605-87-8)
• EPA Substance Registry System: 3-HYDROXY-PHENANTHRENE(605-87-8)

Safety Data

• Hazardous Substances Data: 605-87-8(Hazardous Substances Data)

Usage

Chemical Properties

Tan Solid

Uses

3-Phenanthrol is a metabolite of Phenanthrene.

InChI:InChI=1/C14H10O/c15-12-8-7-11-6-5-10-3-1-2-4-13(10)14(11)9-12/h1-9,15H

Upstream product

• 6335-83-7 4-(2-phenylethyl)phenol 
• 54125-02-9 danishefsky's diene 
• 86-57-7 1-Nitronaphthalene 
• 55149-84-3 2-nitroveratraldehyde 
• 85-01-8 phenanthrene 
• 64-17-5 ethanol 

Downstream Products

• 10386-43-3 4-Formyl-3-phenanthrol 
• 98681-92-6 4-(3-hydroxy-[4]phenanthrylazo)-benzenesulfonic acid 
• 4120-78-9 N-(phenanthren-3-yl)acetamide 
• 4733-11-3 phenanthrene 3,4-quinone 
• 1892-54-2 3-aminophenanthrene 
• 5346-01-0 1-(6-acetoxy-[3]phenanthryl)-ethanone 
• 100780-04-9 (-)-(R)-3,3'-dihydroxy-4,4'-biphenanthrene 
• 74877-24-0 2,2-dihydroxybenzindan-1,3-dione 
• 94688-54-7 Phenyl-phenanthryl-⁽³⁾-aether 
• 116131-75-0 benzoic acid-(4,9-dichloro-[3]phenanthryl ester) 
• 145372-06-1 (aR)-2,2'-dihydroxy-6,6'-dimethoxy-1,1'-binaphthyl 
• 7402-91-7 3-hydroxy-9-nitrophenanthrene 

Relevant articles and documents

Photocatalysis in dimethyl carbonate green solvent: Degradation and partial oxidation of phenanthrene on supported TiO2

Dimethyl carbonate (DMC) is here proposed-for the first time-as a green organic solvent for photocatalytic synthesis. In this work, the photocatalytic partial oxidation of phenanthrene in dimethyl carbonate (DMC) by using anatase TiO2as the photocatalyst is described as paradigmatic example of a green synthetic process starting from polycyclic aromatic hydrocarbons (PAHs). For comparison, the same reaction carried out also in ethanol, 1-propanol or 2-propanol is reported. The use of DMC as the solvent allowed us to achieve 19% and 23% selectivity towards 9-fluorenone and 6H-benzo[c]chromen-6-one, respectively. The proposed approach may represent both a new green synthetic process and an environmentally friendly route to degradation of PAHs. This journal is

Nitronaphthalenes as Diels-Alder dienophiles

1-Nitronaphthalene, 2-nitronaphthalene and 1,3-dinitronaphthalene react with Danishefsky diene as normal electron demand Diels-Alder dienophiles to give hydroxyphenanthrene derivatives as principal products in reasonable yields. The aromatization is an ex

Modification of the Free-Radical Thermolysis of Bibenzyl by Surface Immobilization

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