10040-91-2

Usage

Uses

Used in Personal Care Products and Cosmetics:
5-(3,4-Dimethoxybenzylidene)hydantoin is used as an antimicrobial agent for its ability to inhibit the growth of a broad spectrum of microorganisms. This application helps maintain the safety and efficacy of personal care products and cosmetics, preventing spoilage and contamination.
Used in Preservative Formulations:
As a preservative, 5-(3,4-Dimethoxybenzylidene)hydantoin is used to extend the shelf life of various consumer products. Its strong antimicrobial activity ensures the prevention of microbial growth, thus protecting the products from spoilage and ensuring their quality over time.
Used in Enhancing Product Safety:
5-(3,4-Dimethoxybenzylidene)hydantoin is used as a safety enhancer in consumer products, reducing the risk of infections and allergic reactions caused by microbial contamination. Its compatibility with other ingredients allows for its incorporation into various formulations without affecting the product's performance or quality.
Used in the Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its antimicrobial properties, 5-(3,4-Dimethoxybenzylidene)hydantoin could potentially be used in the pharmaceutical industry as an antimicrobial agent in various applications, such as in the preservation of pharmaceutical formulations or as a component in the development of new antimicrobial drugs.
Used in Research and Development:
5-(3,4-Dimethoxybenzylidene)hydantoin may also be utilized in research and development settings to study its antimicrobial properties and explore its potential applications in various fields, including medicine, agriculture, and environmental protection. This could lead to the discovery of new uses and formulations that leverage its unique characteristics.

InChI:InChI=1/C12H12N2O4/c1-17-9-4-3-7(6-10(9)18-2)5-8-11(15)14-12(16)13-8/h3-6H,1-2H3,(H2,13,14,15,16)/b8-5-

Upstream product

• 461-72-3 2,4-imidazolidinedione 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 253786-51-5 C₁₃H₁₄N₂O₃S 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 32255-79-1 2-hydroxy-3-(3,4-dimethoxyphenyl)propanoic acid 
• 32161-30-1 (S)-3,4-dimethoxyphenylalanine 
• 2460-33-5 3,4-dimethoxyphenylpyruvic acid 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of L-3,4-dimethoxyphenyl-alanine and its analogues using aspartate aminotransferase as a key catalyst

In this study, a chemoenzymatic synthesis method for the production of L-3,4-dimethoxyphenyl-alanine and its analogues from phenylpyruvate derivatives was developed. The aspartate aminotransferase from Escherichia coli was engineered by error prone PCR and the improved variants were identified. When 3, 4-dimethoxy phenylpyruvate was added by fed-batch on a preparative scale, L-3,4-dimethoxyphenyl-alanine was formed in 95.4% conversion and > 99% ee with the best aspartate aminotransferase variant as the catalyst. This study provided an efficient method for the production of methoxy substituted phenylalanines using the engineered aspartate aminotransferase.

Expedient base-mediated desulfitative dimethylamination, oxidation, or etherification of 2-(Methylsulfanyl)-3,5-dihydro-4 H -imidazol-4-one scaffolds

The dimethylamino functionality is generally introduced onto the 3,5-dihydro-4H-imidazol-4-one skeleton by treatment of a halogenated derivative with low-boiling dimethylamine at a high temperature and pressure. The corresponding aliphatic ethers are usua

Antiviral 5-(substituted benzal) hydantoins

Therapeutic compositions containing a compound of the formula: STR1 wherein: R1, R2, and R3 are each hydrogen, hydroxy, alkoxyf 1 to 4 carbon atoms, acyloxy of 1 to 4 carbon atoms, halo, or nitro, or R2 and Rsu