64164-99-4

Usage

Uses

Used in Pharmaceutical Industry:
2-[4-(1,1-dimethylpropyl)benzoyl]benzoic acid is used as an anti-inflammatory and analgesic agent for the treatment of pain, inflammation, and stiffness caused by conditions such as arthritis. It is effective in reducing the production of inflammatory chemicals in the body, thereby alleviating symptoms of pain and discomfort.
Used in Pain Management:
2-[4-(1,1-dimethylpropyl)benzoyl]benzoic acid is used as a pain reliever for managing acute pain or for the long-term management of chronic conditions. It is available in various forms, including oral tablets, topical gels, and suppositories, and is often prescribed for short-term use to manage acute pain or for long-term management of chronic conditions.
Used in Inflammation Reduction:
2-[4-(1,1-dimethylpropyl)benzoyl]benzoic acid is used as an inflammation reducer to help alleviate symptoms of inflammation caused by various conditions. It is effective in reducing the production of inflammatory chemicals in the body, which helps to alleviate symptoms of inflammation and discomfort.

InChI:InChI=1/C19H20O3/c1-4-19(2,3)14-11-9-13(10-12-14)17(20)15-7-5-6-8-16(15)18(21)22/h5-12H,4H2,1-3H3,(H,21,22)

Upstream product

• 85-44-9 phthalic anhydride 
• 2049-95-8 tery-amylbenzene 
• 97-93-8 triethylaluminum 
• 563-43-9 ethylaluminum dichloride 

Downstream Products

• 32588-54-8 2-tert-amylanthraquinone 

Relevant academic research and scientific papers

Friedel - gram acylating reaction method based on phthalic anhydride and aromatic alkyl compound

A part of a substituted alkylbenzene is used as a solvent and a reaction raw material for - gram acylating reaction, a part of a substituted alkylbenzene is dissolved in a reaction raw material phthalic anhydride and a chloroaluminate ionic liquid catalyst, and a residual part of a substituted alkylbenzene is added dropwise - to obtain - (2 - 4' - alkylbenzoyl) benzoic acid intermediate. 2 -position positioning selectivity of the method is higher, and the reaction production cost is low.

Method for synthesizing 2-alkylanthraquinone

The invention discloses a method for synthesizing 2-alkylanthraquinone. The method comprises the following steps: preparing a tert-butylanthraquinone intermediate BE acid from phthalic anhydride and alkylbenzene in the presence of a Lewis acid, carrying out dehydration ring closure by adopting a combined dehydrating agent composed of polyphosphoric acid and phosphorus pentoxide, pouring the obtained solution into ice water after the end of the ring closure I order to dilute the polyphosphoric acid to a certain concentration, adding xylene for extraction after water precipitation is finished, washing and concentrating the obtained extract to obtain a brown yellow block solid, and recrystallizing the solid to obtain the 2-alkylanthraquinone. The method of the invention the advantages of avoiding of using of fuming sulfuric acid and production of a large amount of dilute sulfuric acid in the phthalic anhydride method production process of anthraquinone, easily available raw materials, mild reaction conditions, easiness in application in industrial production, realization of continuous using of the byproduct phosphoric acid as the dehydrating agent after addition of phosphorus pentoxide, and good environmental protection meaning.

Acylation of aromatics

Aromatics are acylated by the Friedel-Crafts method by carrying out the acylation in the presence of metalalkyls or metalalkyl halides of metals or semimetals of main groups two to five and/or of metals of subgroups two or four of the Periodic Table.