607-42-1

Basic information

• Product Name: 1-ANTHRACENECARBOXYLIC ACID
• Synonyms: 1-ANTHRACENECARBOXYLIC ACID;1-Anthracenecarboxilic acid;1-anthroic acid;anthracene-1-carboxylic acid
• CAS NO: 607-42-1
• Molecular Formula: C₁₅H₁₀O₂
• Molecular Weight: 222.24
• Product Categories: Anthracenes
• Mol File: 607-42-1.mol
• Article Data: 11

Chemical Properties

• Melting Point: 252 °C
• Boiling Point: 323.41°C (rough estimate)
• Flash Point: 206.1 °C
• Appearance: /
• Density: 1.1404 (rough estimate)
• Vapor Pressure: 1.53E-09mmHg at 25°C
• Refractive Index: 1.7430 (estimate)
• Storage Temp.: Refrigerator, under inert atmosphere
• Solubility: DMSO (Slightly)
• PKA: pK1: 3.68 (25°C)
• CAS DataBase Reference: 1-ANTHRACENECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1-ANTHRACENECARBOXYLIC ACID(607-42-1)
• EPA Substance Registry System: 1-ANTHRACENECARBOXYLIC ACID(607-42-1)

Safety Data

• Hazardous Substances Data: 607-42-1(Hazardous Substances Data)

Usage

General Description

1-Anthracenecarboxylic Acid is a chemical compound that has been derived from anthracene, a hydrocarbon found in coal tar. It is often used in the development of dyes and pigments due to its ability to produce different colors under various conditions. 1-ANTHRACENECARBOXYLIC ACID is also used in research industries, particularly in the field of organic chemistry, for synthesizing other compounds, testing reactions and gaining further understanding of chemical behaviors. While specific toxicity information on 1-Anthracenecarboxylic Acid is not thoroughly studied, as with any chemical, it should be handled with care to avoid potential health risks.

InChI:InChI=1/C15H10O2/c16-15(17)13-7-3-6-12-8-10-4-1-2-5-11(10)9-14(12)13/h1-9H,(H,16,17)

Upstream product

• 1336-21-6 ammonium hydroxide 
• 602-69-7 anthraquinone-1-carboxylic acid 
• 120-12-7 anthracene 
• 7396-21-6 1-acetylanthracene 
• 38366-32-4 1-cyanoanthraquinone 
• 602-82-4 3-benzoylphthalic acid 
• 7477-59-0 1-chloro-4-methylanthraquinone 
• 82-05-3 7H-benz[d,e]anthracene-7-one 
• 72307-79-0 1-ethynyl-9,10-anthraquinone 
• 82-44-0 1-chloroanthracene-9,10-dione 
• 329686-93-3 N-(1-anthroyloxy)-9-fluorenylideneamine 
• 6268-10-6 4-chloro-9,10-dioxo-9,10-dihydro-1-anthracenecarboxylic acid 
• 7664-41-7 ammonia 
• 3752-42-9 anthracene-1-carbonitrile 

Downstream Products

• 7396-21-6 1-acetylanthracene 
• 25308-58-1 methyl anthranylate 
• 3752-42-9 anthracene-1-carbonitrile 
• 120-12-7 anthracene 
• 1377575-70-6 N-cyclohexyl-N-[(cyclohexylamino)carbonyl]-1-anthracenecarboxamide 
• 1258852-64-0 C₁₅H₁₀O₂*C₄₄H₈₃NO₄ 
• 1258852-62-8 C₁₅H₁₀O₂*C₄₅H₈₅NO₄ 
• 1564-52-9 anthracen-1-yl(phenyl)methanone 
• 861075-95-8 1-(α-hydroxy-benzhydryl)-anthraquinone 
• 859938-60-6 Hydroxy-diphenyl-(9.10-dihydro-anthryl-⁽¹⁾)-methan 
• 132653-13-5 1-benzhydryl-anthraquinone 
• 859074-03-6 1-benzhydryl-9,10-dihydro-anthracene 
• 876483-46-4 9-phenyl-naphth[3,2,1-de]anthracen-5-one 
• 160003-59-8 3-((R)-1-Anthracen-1-yl-2,2-dimethyl-propoxy)-6-chloro-pyridazine 

Relevant articles and documents

1 - [...] synthetic preparation method

The invention discloses a 1 - [...] synthetic preparation method, comprises the following steps: S1) will anthracene and acetyl chloride is dissolved in the solvent, and the catalysis of a Lewis acid, reaction to obtain the 1 - b [...]; S2) 1 - b [...] through oxidation reaction, to obtain 1 - carboxylic acid anthracene; S3) under the action of the acyl, firstly the 1 - anthracene acid radical chloride acid, to remove the surplus solvent, followed by reaction with cyanide, to produce the target compound 1 - cyanate anthracene. The present invention provides 1 - [...] synthetic preparation method, in order to low-cost transfer catalyst, acetyl chloride as the raw material, after three step synthesis of simple and convenient operation, and then after treatment and purification, can prepare and get the purity 98% or more of 1 - [...], not only the production cost is low, the experimental steps are few, simple operation, and after the simple purification, the purity can reach 98% above, can fully meet the T - 2 toxin of the derivatization detection, greatly reduce the T - 2 toxin detection cost.

Use of Mineral/Organic Composite Material in the Form of an Ultraviolet Radiation Protective Agent

The invention relates to the use of composite material which comprises nanoparticles of a least one metal derivative and at least one organic sunscreen agent which is chemically bound with said particles in a covalent manner in the form of an ultraviolet radiation protective agent containing the inventive composite material. Cosmetic ultraviolet radiation protective compositions comprises said mixture are also disclosed.

Synthesis, DNA-damaging and cytotoxic properties of novel topoisomerase II-directed bisantrene analogues

New bisantrene analogues were synthesized, bearing one or two 4,5-dihydro-1H-imidazol-2-yl hydrazone side chains at positions 1,4 or 9 of the anthracene ring system. A 10-aza-bioisostere was also prepared. The position of substituents in structurally isomeric drugs modulates topoisomerase II poisoning and specificity, along with cytotoxicity.