529-86-2

Basic information

• Product Name: anthracen-9-ol
• Synonyms: 9-Anthracenol (9CI); 9-Anthrol (8CI); Anthracene, 9-hydroxy-
• CAS NO: 529-86-2
• Molecular Formula: C₁₄H₁₀O
• Molecular Weight: 194.2286
• Mol File: 529-86-2.mol

Chemical Properties

• Melting Point: 120° (if bath is heated to 110°); mp 152° (if bath is cold at start)
• Boiling Point: 404.5°C at 760 mmHg
• Flash Point: 197.7°C
• Density: 1.244g/cm³
• Vapor Pressure: 4.02E-07mmHg at 25°C
• Refractive Index: 1.753
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 9.40±0.30(Predicted)
• Water Solubility: 35.93mg/L(25 oC)
• CAS DataBase Reference: anthracen-9-ol(CAS DataBase Reference)
• NIST Chemistry Reference: anthracen-9-ol(529-86-2)
• EPA Substance Registry System: anthracen-9-ol(529-86-2)

Safety Data

• Hazardous Substances Data: 529-86-2(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
Anthracen-9-ol is used as a chemical intermediate for the synthesis of various organic compounds. Its solubility in organic solvents and ability to change to anthrone make it a versatile building block in the chemical industry.
Used in Fluorescent Markers:
Due to its blue fluorescence property, anthracen-9-ol is used as a fluorescent marker in research and diagnostic applications. This allows for the detection and tracking of specific molecules or cellular components in various biological studies.
Used in Combustion Applications:
Given its combustible nature, anthracen-9-ol can be utilized in the development of new combustion technologies or as an additive to enhance the combustion properties of certain fuels.
Used in Pharmaceutical Research:
Anthracen-9-ol's unique chemical properties may also make it a candidate for pharmaceutical research, potentially leading to the development of new drugs or drug delivery systems.
Used in Material Science:
anthracen-9-ol's crystalline structure and solubility characteristics could be exploited in material science for the creation of new materials with specific optical or electronic properties.

Upstream product

• 602-60-8 9-nitroanthracene 
• 120-12-7 anthracene 
• 79755-94-5 4a-acetyl-1,4,4a,9,9a,10-hexahydro-9,10-o-benzenoanthracene-1,4-dione 
• 76-05-1 trifluoroacetic acid 

Downstream Products

• 53781-03-6 10-(4-methoxy-benzyliden)-anthrone 
• 98782-44-6 (10H-[9]anthrylidene)-phenyl-amine 
• 5447-86-9 10,10-dimethyl-9,10-dihydroanthracen-9-one 
• 434-85-5 bianthrone 
• 779-02-2 9-methylanthracene 
• 100606-13-1 10-(α-chlorobenzylidene)anthrone 
• 740838-63-5 10,10-bis-(4-dimethylamino-phenyl)-anthrone 
• 408317-53-3 9,10-dibenzyl-9,10-dihydro-anthracene-9,10-diol 
• 96555-79-2 9a,10-dibenzoyl-4b,9,9a,10-tetrahydro-9-oxo-cis-indeno<1,2-a>indene 
• 579504-87-3 10-(3,4,5-trimethoxybenzyl)-9(10H)-anthracenone 
• 579504-84-0 10-(3,5-dimethoxybenzyl)-9(10H)-anthracenone 
• 579504-79-3 10-(4-methoxybenzyl)-9(10H)-anthracenone 
• 16603-23-9 10-benzyl-9(10H)-anthracenone 
• 1498-71-1 9-benzylanthracene 

Relevant articles and documents

Efficient oxidation of polycyclic aromatic hydrocarbons with H 2O2 catalyzed by 5,10,15-triarylcorrolatoiron (IV) chloride in ionic liquids

A simple and efficient oxidative system has been developed for the oxidation of polycyclic aromatic hydrocarbons with H2O2 catalyzed by 5,10,15-triarylcorrolatoiron (IV) chloride in mixed reaction media using imidazolium ionic liquids and organic solvents. The coordination effects of different organic solvents as well as anions of ionic liquids on the oxidation reactions have been examined.

Photocatalytic degradation of polycyclic aromatic hydrocarbons in GaN:ZnO solid solution-assisted process: Direct hole oxidation mechanism

GaN:ZnO exhibits excellent activity for the photodegradation of PAHs, and the activity can be obviously improved by loading Pt. The degradation of PAHs in the system of GaN:ZnO is induced by the formation of holes. The holes generated then interact with PAHs to produce PAHs+, which is active enough to react with O2.

Photophysics and Photochemistry of Nitroanthracenes. Part 2. Primary Process in the Photochemical Reaction of 9-Nitroanthracene studied by Steady-state Photolysis and Laser Photolysis

From measurements of phosphorescence and triplet-triplet absorption spectra of the lowest excited triplet ??* state of 9-nitroanthracene (NA) together with the absorption spectrum of 9-anthryloxy radical, it is concluded that photolysis of 9-nitroanthracene gives rise to the nitro -> nitrite rearrangement for a higher excited triplet state of n?* character, followed by the cleavage of 9-anthryl nitrite to 9-anthryloxy radical and nitrogen(II) oxide, yielding 9-anthrol (and anthrone), 10,10'-bianthrone and 9-nitrosoanthrone in ethanol; and 10,10'-bianthrone and 9-nitrosoanthrone in benzene.Hence, the primary process in the photochemical reaction of NA is essentially identical with those of 9-benzoyl-10-nitroanthracene and 9-cyano-10-nitroanthracene except that no 10,10'-bianthrone derivatives are formed.

Benzoquinones and Related Compounds. Part 4. Thermolysis of the Diels-Alder Adduct of 2-Acetyl-5,6-dichloro-1,4-benzoquinone and Cyclopentadiene: Evidence for a Partial Retro-diene Reaction

Addition of chlorine to (2-methyl-1,3-dioxolan-2-yl)-1,4-benzoquinone occurs at the unsubstituted double bond.Subsequent enolisation and cleavage of the acetal affords 2-acetyl-5,6-dichlorohydroquinone in 50percent overall yield.Oxidation of this gives the corresponding 1,4-benzoquinone which with cyclopentadiene yields, predominantly, the 1 : 1 Diels-Alder adduct (6) by endo-addition to the 2,3-double bond.Thermolysis of this adduct in benzene results in disproportionation to cyclopentadiene and the spiro-acetal (13); thermolysis in acetic acid also yields (13), but the major product is the dihydrobenzofuran (14), an isomer of the Diels-Alder adduct.Mechanisms for the formation of these products are discussed.