610-50-4

Basic information

• Product Name: 1-HYDROXYANTHRACENE
• Synonyms: 1-HYDROXYANTHRACENE;1-Anthracenol;Anthracen-1-ol
• CAS NO: 610-50-4
• Molecular Formula: C₁₄H₁₀O
• Molecular Weight: 194.23
• Mol File: 610-50-4.mol
• Article Data: 11

Chemical Properties

• Melting Point: 158°C
• Boiling Point: 290.68°C (rough estimate)
• Appearance: /
• Density: 1.0550 (rough estimate)
• Refractive Index: 1.5500 (estimate)
• CAS DataBase Reference: 1-HYDROXYANTHRACENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-HYDROXYANTHRACENE(610-50-4)
• EPA Substance Registry System: 1-HYDROXYANTHRACENE(610-50-4)

Safety Data

• Hazardous Substances Data: 610-50-4(Hazardous Substances Data)

Usage

General Description

1-Hydroxyanthracene is a chemical compound with the molecular formula C14H10O. It is a primary metabolite of anthracene, a polycyclic aromatic hydrocarbon commonly found in coal tar and fossil fuels. 1-Hydroxyanthracene is known to be a mutagen and a potential carcinogen, as it can induce DNA damage in cells. It is also used as a precursor in the synthesis of various dyes, pigments, and pharmaceuticals. The compound is classified as a hazardous substance by the Environmental Protection Agency (EPA) and should be handled with caution due to its toxic and potentially harmful effects on human health and the environment.

Upstream product

• 610-49-1 1-aminoanthracene 
• 64-17-5 ethanol 
• 4985-70-0 1-chloroanthracene 
• 142-71-2 copper diacetate 
• 127-09-3 sodium acetate 
• 54458-84-3 1-methoxyanthracene 
• 82-34-8 1-nitroanthraquinone 
• 22187-13-9 1,4-dihydro-1,4-epoxyanthracene 
• 129-43-1 1-hydroxyanthraquinone 
• 1286756-63-5 1-hexyloxyanthracene 
• 82-49-5 1-anthraquinonesulfonic acid 
• 82-45-1 1-amino-9,10-anthracenedione 
• 577-94-6 (+)-trans-1,2-dihydro-anthracene-1,2-diol 
• 70411-24-4 1,2-anthracene oxide 

Downstream Products

• 610-49-1 1-aminoanthracene 
• 54458-84-3 1-methoxyanthracene 
• 91097-74-4 4-(4-hydroxy-[1]anthrylazo)-benzenesulfonic acid 
• 5440-71-1 3,4,5,6,7,8-hexahydro-1(2H)-anthracenone 
• 2141-42-6 1,2,3,4-tetrahydroanthracene 
• 54784-07-5 3,4-dihydro-2H-anthracen-1-one 
• 1356382-62-1 3-(4-methoxyphenyl)-3,4-dihydro-2H-anthra[2,1-e]-1,3-oxazine 
• 1356382-63-2 3-(4-methylphenyl)-3,4-dihydro-2H-anthra[2,1-e]-1,3-oxazine 
• 1356382-64-3 3-phenyl-3,4-dihydro-2H-anthra[2,1-e]-1,3-oxazine 
• 1356382-65-4 3-(4-chlorophenyl)-3,4-dihydro-2H-anthra[2,1-e]-1,3-oxazine 
• 1220282-45-0 N-(anthracen-2-yl)benzylamine 
• 1569905-79-8 tert-butyl N-[3-(1-{3-[(4R)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]-3-oxopropyl}anthracen-2-yl)propyl]carbamate 
• 113061-88-4 4-phenylazo-[1]anthrylamine 
• 635-12-1 1,4-anthraquinone 

Relevant articles and documents

Direct formation of fullerene monolayers using [4+2] Diels-Alder cycloaddition

The formation of covalent C60 monolayers through [4+2] Diels-Alder cycloaddition between C60 and anthracene monolayers grafted onto a silicon oxide surface was investigated by ellipsometry, fluorescence and by atomic force microscopy.

Preparation of anthryl diethylene glycol monomethyl ether and identification of potassium ions

Provided is a preparation method for an anthryl diethylene glycol monomethyl ether compound. The compound is synthesized by using 1-aminoanthraquinone and chlorodiethylene glycol monomethyl ether as starting materials. Based on an ether chain and potassiu

Synthesis of Naphthyl-, Quinolin- and Anthracenyl Analogues of Clofibric Acid as PPARα Agonists

PPARα is a ligand activated transcription factor belonging to the nuclear receptor subfamily, involved in fatty acid metabolism in tissues with high oxidative rates such as muscle, heart and liver. PPARα activation is important in steatosis, inflammation and fibrosis in preclinical models of non-alcoholic fatty liver disease identifying a new potential therapeutic area. In this work, three series of clofibric acid analogues conjugated with naphthyl, quinolin, chloroquinolin and anthracenyl scaffolds were synthesized. In an effort to obtain new compounds active as PPARα agonists, these molecules were evaluated for PPARα transactivation activity. Naphthyl and quinolin derivatives showed a good activation of PPARα; noteworthy, optically active naphthyl derivatives activated PPARα better than corresponding parent compound.