607-42-1

Usage

Uses

Used in Dye and Pigment Industries:
1-Anthracenecarboxylic Acid is used as a key component in the development of dyes and pigments for its ability to produce different colors under various conditions. This property makes it a valuable asset in creating a wide range of colorants for various applications.
Used in Research Industries:
1-Anthracenecarboxylic Acid is used as a research chemical in the field of organic chemistry. It serves as a starting material for synthesizing other compounds, testing reactions, and gaining a deeper understanding of chemical behaviors. This application is crucial for advancing scientific knowledge and developing new chemical processes.

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

• 3752-42-9 anthracene-1-carbonitrile 
• 82-05-3 7H-benz[d,e]anthracene-7-one 
• 120-12-7 anthracene 
• 7396-21-6 1-acetylanthracene 
• 1336-21-6 ammonium hydroxide 
• 602-69-7 anthraquinone-1-carboxylic acid 
• 38366-32-4 1-cyanoanthraquinone 
• 602-82-4 3-benzoylphthalic acid 
• 7477-59-0 1-chloro-4-methylanthraquinone 
• 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 

Downstream Products

• 25308-58-1 methyl anthranylate 
• 1564-52-9 anthracen-1-yl(phenyl)methanone 
• 1258852-62-8 C₁₅H₁₀O₂*C₄₅H₈₅NO₄ 
• 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 
• 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 
• 172787-84-7 (S)-1-(1-anthryl)-2,2-dimethylprop-1-yl 6-chloro-3-pyridazyl ether 

Relevant academic research and scientific papers

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.

1-(Methylamino)anthracene – An Accessible Building Block for Photoresponsive Compounds

In this paper we present a convenient and scalable synthesis of 1-(methylamino)anthracene, which is a potent building block for the construction of photoresponsive materials. With this structural motif we have synthesized an anion receptor bearing two anthracene groups. Interaction of a chloride anion with the anthracene moieties increases the association constant. Photocycloaddition allows to obtain a single macrocyclic receptor, which exhibits higher binding constants due to the macrocyclic effect.

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.

Mechanism for photocleavage of N-(anthroyloxy)-9-fluorenylideneamines and dynamic behavior of anthroyloxyl radicals

Photocleavage of the N-O bond of N-(9-anthroyloxy)-9-fluorenylideneamine and its 1-and 2-anthroyloxy derivatives takes place efficiently in acetonitrile in the excited singlet state attributed to the fluorenylidene moiety. This made it possible for the first time to directly observe anthroyloxyl radicals by the transient absorption method. The quantum efficiency for photocleavage decreases remarkably in benzene, in which the lowest excited singlet state is attributed to the anthroate moiety. All the three kinds of anthroyloxyl radicals are much less reactive in decarboxylation, addition to olefins, and hydrogen-atom abstraction than benzoyloxyl and 1- and 2-naphthoyloxyl radicals; 9-anthroyloxyl radicals supposedly undergo intramolecular addition-elimination in the ipso-position in equilibrium with α-lactonic spirodihydroanthryl radicals, as indicated by one-color and two-color laser photolyses.

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.

Photoisomerization and Photocyclization Reactions of 1-Styrylanthracene

On triplet sensitization, 1-styrylanthracene (1SA) undergoes adiabatic cis->trans one-way isomerization (3c*->3t*) similarly to 2-anthrylethylenes.However, upon direct irradiation, cis-1SA in the singlet excited state mostly undergoes cyclization to a dihydrophenanthrene-type product (DHP), 4a,4b-dihydrobenzochrysene, competing with an inefficient intersystem crossing to 3c* followed by one-way isomerization.The produced DHP, in deaerated benzene, is reverted to cis-1SA by a thermal (Ea = 14.9 kcal mol-1) or a photochemical pathway; however, under an oxygenated atmosphere DHP gives benzochrysene.A failure in the production of a cyclized product upon the excitation of trans-1SA shows that the isomerization really takes place in a one-way fashion.

2-[(arylmethyl)amino]-2-methyl-1,3-propanediol DNA intercalators. An examination of the effects of aromatic ring variation on antitumor activity and DNA binding

The effects of variation of aromatic ring size, shape, and side-chain position on antitumor activity and DNA binding in a series of carbocyclic 2-[(arylmethyl)amino]-2-methyl-1,3-propanediols (AMAPs) were examined. In general, the interaction of AMAPs wit

COMPLEXATION OF AROMATIC CARBOXYLIC ACIDS WITH HEPTAKIS(2,6-DI-O-METHYL)CYCLOMALTOHEPTAOSE IN CHLOROFORM AND WATER

Complexation of various aromatic carboxylic acids with heptakis(2,6-di-O-methyl)cyclomaltoheptaose (DM-βCD) in chloroform and water has been studied by u.v. absorption, induced c.d., and n.m.r. spectroscopy.The inclusion complex of dimethylaminobenzoic acid is axial in water but equatorial or lid-type in chloroform, that of anthracene-9-carboxylic acid is axial in water and equatorial in chloroform, that of pyrene-1-carboxylic acid is lid-type in water at pH 9.0, and that of ferrocenecarboxylic acid depends on the dissociation of the carboxyl group.

Anthracene derivatives

The present invention relates to compounds of formula (I) or a monomethyl or a monoethyl ether thereof (the compound of formula (I) including these ethers may contain no more than 30 carbon atoms in total); ethers, esters thereof; acid addition salts thereof; wherein Ar is an anthracene or substituted anthracene ring system; R1 contains not more than eight carbon carbon atoms and is a group STR1 wherein m is 0 or 1; R5 is hydrogen; R6 and R7 are the same or different and each is hydrogen or C1-3 alkyl optionally substituted by hydroxy; R8 and R9 are the same or different and each is hydrogen or C1-3 alkyl; --C--C-- is a five- or six-membered saturated carbocyclic ring; R10 is hydrogen, methyl or hydroxymethyl; R11, R12 and R13 are the same or different and each is hydrogen or methyl; R14 is hydrogen, methyl, hydroxy, or hydroxymethyl.

Pigment composition

A pigment composition contains a pigment and a dispersant. The dispersant is a phosphoric ester compound represented by the following general formula: wherein at least one of the three Rs is a residuum of a polyester chain containing as principal bonds thereof ester bonds of a polycarboxylic acid and a polyalcohol.