116-83-6

Basic information

• Product Name: 1-amino-4-methoxyanthracene-9,10-dione
• Synonyms: 1-amino-4-methoxyanthracene-9,10-dione;BRN 2218945;1-Amino-4-methoxy-9,10-anthraquinone;1-azanyl-4-methoxy-anthracene-9,10-dione
• CAS NO: 116-83-6
• Molecular Formula: C₁₅H₁₁NO₃
• Molecular Weight: 253.25274
• Mol File: 116-83-6.mol
• Article Data: 6

Chemical Properties

• Melting Point: 171 °C
• Boiling Point: 502°Cat760mmHg
• Flash Point: 274.9°C
• Appearance: /
• Density: 1.366g/cm³
• Vapor Pressure: 3.3E-10mmHg at 25°C
• Refractive Index: 1.674
• PKA: 0.21±0.20(Predicted)
• CAS DataBase Reference: 1-amino-4-methoxyanthracene-9,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-amino-4-methoxyanthracene-9,10-dione(116-83-6)
• EPA Substance Registry System: 1-amino-4-methoxyanthracene-9,10-dione(116-83-6)

Safety Data

• Hazardous Substances Data: 116-83-6(Hazardous Substances Data)

Usage

General Description

1-amino-4-methoxyanthracene-9,10-dione is a chemical compound that belongs to the family of anthracene derivatives. It has a molecular formula of C15H11NO3 and a molecular weight of 253.25 g/mol. 1-amino-4-methoxyanthracene-9,10-dione is a synthetic dye intermediate that is commonly used in the production of dyestuffs and pigments. It is also involved in the synthesis of various pharmaceuticals and other organic compounds. Additionally, 1-amino-4-methoxyanthracene-9,10-dione has been studied for its potential biological activities, including its role as a cytotoxic agent, as well as its potential use in photodynamic therapy for cancer treatment. Overall, this compound has widespread applications in the chemical, pharmaceutical, and medical industries.

InChI:InChI=1/C15H11NO3/c1-19-11-7-6-10(16)12-13(11)15(18)9-5-3-2-4-8(9)14(12)17/h2-7H,16H2,1H3

Upstream product

• 771-60-8 2,3,4,5,6-pentafluoroaniline 
• 126628-19-1 C₁₅H₁₀NO₃^(1-)*Na⁽¹⁺⁾ 
• 6409-75-2 1-benzamido-4-methoxy-9,10-anthraquinone 
• 82-39-3 1-methoxyanthracene-9,10-dione 
• 25022-95-1 1-chloro-4-methoxy-anthraquinone 
• 70730-92-6 5-chloro-6H-anthra[1,9-cd]isoxazol-6-one 
• 116-85-8 4-hydroxy-1-aminoanthraquinone 
• 74-88-4 methyl iodide 
• 85192-90-1 5-methoxy-6-oxo-6H-anthra<1,9-cd>isoxazole 
• 102452-22-2 N-(4-methoxy-9,10-dioxo-9,10-dihydro-[1]anthryl)-toluene-4-sulfonamide 
• 81-66-3 1-methoxy-4-nitro-anthraquinone 

Downstream Products

• 85193-15-3 1-S,S-diphenyl-N-(4-methoxyanthraquinon-1-yl)sulfoximide 
• 159389-42-1 2-bromo-1-(2-cyclohexenecarboxamido)-4-methoxyanthraquinone 
• 159389-38-5 2-bromo-1-(1'-cyclohexenecarboxamido)-4-methoxyanthraquinone 
• 159389-36-3 1-(1'-cyclohexenecarboxamido)-4-methoxyanthraquinone 
• 6370-71-4 2,6-bis-(4-methoxy-9,10-dioxo-9,10-dihydro-[1]anthrylamino)-anthraquinone 
• 2475-44-7 disperse blue 14 
• 1220-94-6 1-amino-4-(methylamino)anthraquinone 
• 159389-37-4 1-(2'-bromo-1'-cyclohexenecarboxamido)-4-methoxyanthraquinone 
• 86226-12-2 1-amino-2-p-dimethylanilino-4-methoxyanthraquinone 
• 771-60-8 2,3,4,5,6-pentafluoroaniline 
• 126628-19-1 C₁₅H₁₀NO₃^(1-)*Na⁽¹⁺⁾ 
• 28949-07-7 1-amino-4-(p-aminoanilino)anthraquinone 
• 4395-65-7 oracet blue 2R 
• 6409-75-2 1-benzamido-4-methoxy-9,10-anthraquinone 

Relevant articles and documents

USE OF INDANTHRENE COMPOUNDS IN ORGANIC PHOTOVOLTAICS

The present invention relates to an organic solar cell which comprises at least one photoactive region which comprises at least one indanthrene compound which is in contact with at least one fullerene compound, and to the use of indanthrene compounds in o

EQUILIBRIUM NH ACIDITY OF 4-SUBSTITUTED 1-AMINOANTHRAQUINONES IN DIMETHYL SULFOXIDE

The equilibrium acidity of 1-amino-4-R-anthraquinones (R = CH3O, H, Cl, Br, NO2) was determined by transmetallation in DMSO (the Na+ cation, 25 deg C).A linear correlation was established between the pK values of the 4-substituted 1-aminoanthraquinones and the ?p- constants of the substituents R.The conduction of the electronic effect of the substituents R is stronger in the aminoanthraquinones than in the anilines and is closer to the naphthylamines.A linear relation is observed between the conduction of the electronic effect of the substituent and the square of the coefficient in the HOMO for the carbon atom at the point of addiion of the substituent in the series of anions of NH acids of various structure types.The increase in the NH acidity with change in the structure type of the NH acid is not necessarily accompanied by a decrease in the conduction of the electronic effect of the substituents.

PHOTOCHEMICAL REACTION OF 9,10-ANTHRAQUINONE AND ITS DERIVATIVES WITH PYRIDINE

The previously unknown photochemical reaction of 9,10-anthraquinone with pyridine in an atmosphere of argon takes place with formation of 2-(1,2-dihydropyridino)- or 2-(1,4-dihydropyridino)-9,10-anthraquinone, which is converted by the action of alkali into 2-aminoanthraquinone.In the presence of atmospheric oxygen the reaction product after treatment whith alkali is 1-aminoanthraquinone in addition to 2-aminoanthraquinone.The 1- and 2-methoxyanthraquinones and chloroanthraquinones react with pyridine in the light and form, after treatment with alkali, substituted aminoanthraquinones.