56776-45-5

Usage

Uses

Used in Dye and Pigment Industry:
2,3'-Dimethylbenzanilide is used as a key intermediate in the synthesis of azo dyes for its ability to contribute to the formation of vibrant and colorfast dyes, which are essential in various industries such as textiles, plastics, and printing inks.
Used in Cosmetic Industry:
2,3'-Dimethylbenzanilide is used as a fragrance and flavoring agent in the cosmetic industry to enhance the sensory appeal of products, providing a pleasant scent or taste that can improve consumer experience.
Used in Food Industry:
Similarly, in the food industry, 2,3'-Dimethylbenzanilide is utilized as a flavoring agent to impart specific tastes to food products, contributing to their overall flavor profile and consumer acceptance.
Used in Pharmaceutical Research:
2,3'-Dimethylbenzanilide is studied for its potential pharmaceutical applications, particularly as an anti-inflammatory and analgesic agent, indicating its possible use in the development of new medications for pain relief and inflammation management.

InChI:InChI=1/C15H15NO/c1-11-6-5-8-13(10-11)16-15(17)14-9-4-3-7-12(14)2/h3-10H,1-2H3,(H,16,17)

Upstream product

• 118-90-1 ortho-methylbenzoic acid 
• 108-44-1 1-amino-3-methylbenzene 
• 933-88-0 ortho-toluoyl chloride 
• 84053-11-2 2-amino-3-(4-mercaptophenyl)propanoic acid 

Downstream Products

• 928151-35-3 2-chloro-2'-methyl-4'-(2-methylbenzoylamino)-acetophenone 
• 928151-36-4 2-chloro-4'-methyl-2'-(2-methylbenzoylamino)aceto-phenone 
• 317374-07-5 2-bromo-5-(2-methylbenzoylamino)toluene 
• 928151-34-2 2-methyl-4-(2-methylbenzoylamino)acetophenone 

Relevant academic research and scientific papers

Method for synthesizing amide compound through photocatalysis in water phase

The invention discloses a method for synthesizing an amide compound through photocatalysis in a water phase. The method comprises the following steps: putting catalysis amounts of a free radical initiator, an amine derivative, a carboxylic acid derivative, a phase transfer catalyst, an inorganic base and water into a reaction container, carrying out a reaction in a photocatalysis reaction instrument at certain power under a room temperature condition, after a certain time, carrying out extraction by using a small amount of ethyl acetate, and carrying out recrystallization, so as to obtain theamide compound, wherein the free radical initiator is eosin, methyl orange, sodium persulfate, ammonium persulfate or potassium peroxodisulfate, the phase transfer catalyst is tetrabutylammonium bromide, and the power of the photocatalytic reaction instrument is 5W. By adopting the method disclosed by the invention, toxic thionyl chloride or phosphorus oxychloride is not needed for a chlorinationreaction, water is adopted as a solvent, a novel photocatalysis method is used, and the amide compound with a high yield can be prepared through a room-temperature reaction for 2-5 hours with an incandescent light bulb of 5W, and in addition, the method is simple in aftertreatment, and low in cost and is an ideal green synthesis method of amide compounds.

PROCESS FOR PREPARING BENZAZEPINE COMPOUNDS OR SALTS THEREOF

This invention provides a process for preparing benzazepine compounds of the formula (1): wherein X1is a halogen atom, R1and R2are a lower alkyl group, or salts thereof as well as intermediate benzoic acid compounds in high yield and high purity on industrial scale, which are useful as an intermediate for preparing a pharmaceutically active 2,3,4,5-tetrahydro-1H-1-benzazepine compound having vasopressin antagonistic activity.