2346-63-6

Usage

Uses

Used in Polymer and Resin Production:
2-(2,4-dimethylbenzoyl)benzoic acid is used as a photoinitiator for the production of polymers and resins. It plays a crucial role in facilitating the curing or hardening of these materials when exposed to light, enhancing their properties and performance in various applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-(2,4-dimethylbenzoyl)benzoic acid is used as a versatile building block for the synthesis of various drugs. Its unique structure allows for the development of new and innovative pharmaceutical compounds with potential therapeutic benefits.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, 2-(2,4-dimethylbenzoyl)benzoic acid serves as a key component in the synthesis of various agrochemicals. Its structural properties enable the creation of new and effective products for agricultural applications.
Used in Organic and Materials Chemistry:
2-(2,4-dimethylbenzoyl)benzoic acid also has potential applications in the field of organic and materials chemistry. Its unique structure and properties make it a valuable chemical for research and development in these areas, contributing to advancements in material science and the discovery of new organic compounds.

Upstream product

• 85-44-9 phthalic anhydride 
• 108-38-3 m-xylene 
• 4397-55-1 phthalic monoacid monomethyl ester chloride 
• 88-95-9 Phthaloyl dichloride 
• 7446-70-0 aluminium trichloride 
• 776279-83-5 2-oxo-2-(2,4-dimethylphenyl)acetic acid 
• 65-85-0 benzoic acid 

Downstream Products

• 93517-75-0 4-(2,4-dimethyl-phenyl)-2H-phthalazin-1-one 
• 95025-68-6 3-(2,4-dimethyl-phenyl)-3-phenyl-3H-isobenzofuran-1-one 
• 380228-07-9 2-(2,4-dimethyl-benzoyl)-benzoic acid amide 
• 2224-80-8 3-(2,4-Dimethylphenyl)-isoindolin-1-on 
• 65-85-0 benzoic acid 
• 611-01-8 2,4-dimethyl-benzoic acid 
• 329922-54-5 4-(2,4-dimethylphenyl)-2-(2-nitro-5-chlorophenyl)-1,2-dihydrophthalazin-1(2H)-one 
• 1055981-49-1 (S)-2-(2',4'-dimethylbenzoyl)-N-(α-phenylethyl)benzamide 
• 388080-46-4 4-(2,4-dimethylphenyl)-2-phenyl-2H-phthalazin-1-one 
• 1392119-82-2 methyl 2-(4-(2,4-dimethylphenyl)-2-methyl-1-oxo-1,2-dihydroisoquinolin-3-yl)-4-methylpentanoate 
• 1392119-76-4 [4-(2,4-dimethylphenyl)-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinyl]acetic acid 
• 1392119-75-3 [4-(2,4-dimethylphenyl)-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinyl]acetonitrile 
• 1392119-74-2 3-(chloromethyl)-4-(2,4-dimethylphenyl)-2-methyl-1(2H)-isoquinolinone 
• 1392119-71-9 4-(2,4-dimethylphenyl)-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinecarboxylic acid 

Relevant academic research and scientific papers

Determination of the Lifetime of the Second Excited Triplet State of Anthracenes

The lifetimes of the T2 states of several substituted anthracenes have been determined using competitive quenching techniques in combination with laser flash photolysis.Thus, Stern-Volmer quenching of 1,3-octadiene yields different slopes depending on whether the triplet or the fluorescence yield are monitored.The difference, which can be treated quantitatively, is the result of T2 quenching by the diene.Typical T2 lifetimes are ca. 23, 11, and 3 ps for 9,10-dichloroanthracene, anthracene, and 1-methylanthracene, respectively.It is shown that consideration of time-dependent diffusional quenching is essential and that discrepancies with earlier studies may largely reflect the contribution from this process, as well as S1 quenching by typical T2 quenchers.Theoretical calculations suggest that interactions of T2 with the nearby T3 state may play a key role in determining the rate of internal conversion to T1.Calculations have been carried out for the methyl derivatives; these, while consistent with experiments, tend to reflect the limitations of current theory in the interpretation of substituent effects.

Ultrasound-promoted Friedel-Crafts acylation of arenes and cyclic anhydrides catalyzed by ionic liquid of [bmim]Br/AlCl3

A simple and efficient method of Friedel-Crafts acylation of arenes with succinic anhydride, phthalic anhydride and glutaric anhydride under the action of 1-butyl-3-ethylimidazolium ([bmim]Br/AlCl3 ([bmim]+) cation (ionic liquid) and ultrasound irradiation is presented. Thy purity of products was tested by GC-MS and their structures evaluated by IR and 1H NMR spectroscopy.

Palladium-catalyzed chemoselective decarboxylative ortho acylation of benzoic acids with α-oxocarboxylic acids

Palladium-catalyzed chemoselective decarboxylative cross coupling of benzoic acids with α-oxocarboxylic acids was realized via an arene sp 2 C-H functionalization process. This work represents the first example of transition-metal-catalyzed cro

ISOQUINOLINE COMPOUNDS AND METHODS FOR TREATING HIV

Provided are compounds and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and their use for treating viral infections mediated by a member of the retrovirus family of viruses such as the Human Immunodeficiency Virus (HIV).

An efficient one-pot synthesis of pyridazinones and phthalazinones using HY-zeolite

Figure represented. The first one-pot synthesis of pyridazinones and phthalazinones from arenes, cyclic anhydrides, and ArNHNH2 in the presence of efficient recyclable heterogeneous catalyst, HY-zeolite, in high yield and short reaction time is reported.

INVESTIGATION OF THE COMPOSITION OF PETROLEUM ANTHRACENE HYDROCARBONS

The optimum conditions of adduct formation with maleic anhydride for the isolation of ca. 100percent anthracene hydrocarbons from a mixture with phenanthrenes and other compounds are set out.Gas-liquid chromatography has been used to study the individual composition of anthracene and C1-C3 anthracenes isolated by the method proposed from concentrates of triaromatic hydrocarbons of crude oils from the Okha, Katangli (Sakhalin) and Dorokhovsk (Urals-Volga) fields.With the aid of the individual compounds synthesized, for the first time 2-ethylanthracene and 1,3- and 2,3-dimethylanthracene have been identified in crude oils, and the retention indices have also been calculated for certain C2- and C3-substituted anthracene hydrocarbons for chromatographic phase SE-54.