91143-76-9

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-O-TOLYL-SUCCINIC ACID serves as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with enhanced therapeutic or pesticidal properties, contributing to the advancement of these industries.
Used in Polymer and Resin Production:
In the field of materials science, 2-O-TOLYL-SUCCINIC ACID is utilized in the production of high-performance polymers and resins. Its incorporation into these materials can improve their mechanical, thermal, and chemical properties, making them suitable for a wide range of applications, including coatings, adhesives, and composites.
Used in Antioxidant and Anti-inflammatory Research:
2-O-TOLYL-SUCCINIC ACID has been studied for its potential antioxidant and anti-inflammatory properties. As a result, it may be used as a therapeutic agent or incorporated into formulations to combat oxidative stress and inflammation, offering new avenues for the treatment of various diseases and conditions.
Environmental and Health Considerations:
2-O-TOLYL-SUCCINIC ACID is considered to have low toxicity, and it is not known to pose significant health or environmental hazards. This makes it a preferred choice for applications where safety and sustainability are paramount, further expanding its potential uses across different industries.

InChI:InChI=1/C11H12O4/c1-7-4-2-3-5-8(7)9(11(14)15)6-10(12)13/h2-5,9H,6H2,1H3,(H,12,13)(H,14,15)

Upstream product

• 932-31-0 ortho-tolylmagnesium bromide 
• 624-48-6 dimethyl cis-but-2-ene-1,4-dioate 
• 15448-24-5 1,1,2-Trimethoxycarbonyl-2-(o-tolyl)-ethan 

Downstream Products

• 610-27-5 4-nitrophthalic acid 
• 1155401-83-4 N-[2-{4-(2-fluorophenyl)-piperazin-1-yl}-ethyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-86-7 N-[2-{4-(3-trifluoromethylphenyl)-piperazin-1-yl}-ethyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-88-9 N-[3-{4-(3-chlorophenyl)-piperazin-1-yl}-propyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-89-0 N-[3-{4-(3-trifluoromethylphenyl)-piperazin-1-yl}-propyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-85-6 N-[2-{4-(3-chlorophenyl)-piperazin-1-yl}-ethyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-87-8 N-[3-{4-(2-methoxyphenyl)-piperazin-1-yl}-propyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-84-5 N-[2-{4-(2-methoxyphenyl)-piperazin-1-yl}-ethyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-82-3 N-[2-(4-phenylpiperazin-1-yl)-ethyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1133-31-9 7-Methyl-3-oxo-indan-1-carbonsaeure 
• 69371-19-3 3-(2-methylphenyl)-pyrrolidine-2,5-dione 

Relevant academic research and scientific papers

Method for synthesizing succinic acid compounds

The invention provides a method for synthesizing succinic acid compounds. The method specifically comprises the following steps: adding a substrate, a photocatalyst and an alkali into a reaction tube,adding a reducing agent and a solvent under the atmosphere of CO2, conducting reacting under the irradiation of visible light, carrying out quenching treatment after the raw materials react completely, and then conducting separating and purifying to obtain a dicarboxylated product of olefin, namely a succinic acid compound. The photocatalyst is 4CzIPN or Ir[(ppy)2(dtbppy)]PF6 and the like, and the reaction substrate comprises 1,1-diaryl ethylene, a monoaryl substituted olefin compound, an acrylate compound and allene. According to the scheme provided by the invention, the reaction conditionsare mild, the applicability of the reaction substrate is wide, and the yield is basically not influenced under the condition that the reaction substrate is amplified to the gram scale; and meanwhile,the invention overcomes the defects of high toxicity of reagents and harsh reaction conditions in the prior art, and has a good industrial application prospect.