5349-85-9

Usage

Uses

Used in Pharmaceutical Industry:
1-(4-chlorophenyl)-5-furan-2-yl-3-thiophen-2-yl-4,5-dihydro-1H-pyrazole is used as a potential therapeutic agent for various medical conditions due to its potential biological activities. 1-(4-chlorophenyl)-5-furan-2-yl-3-thiophen-2-yl-4,5-dihydro-1H-pyrazole's specific application and efficacy would depend on further research and testing, but its pharmacological properties suggest it may have utility in treating inflammation, pain, and fever.
Used in Chemical Research:
In the field of chemical research, 1-(4-chlorophenyl)-5-furan-2-yl-3-thiophen-2-yl-4,5-dihydro-1H-pyrazole serves as a valuable compound for studying the structure-activity relationships of pyrazoles and their derivatives. This can lead to the development of new drugs with improved properties and targeted applications.

Upstream product

• 4128-31-8 rac-octan-2-ol 
• 849585-22-4 LACTIC ACID 

Downstream Products

• 6628-72-4 adipic acid bis-[1-(1-methyl-heptyloxycarbonyl)-ethyl ester] 

Relevant academic research and scientific papers

Synthesis and Evaluation of Surface and Biological Properties of Some Lactic Acid-Based Anionic Surfactants

In the present study, 11 lactic acid-based anionic surfactants were synthesized and evaluated for their surface and biological activities. The synthesis involved the esterification of lactic acid with a range of fatty alcohols differing in chain length as well as in branching and unsaturation. The resultant ester was sulfonated by treatment with chlorosulfonic acid followed by salt formation with aqueous NaOH solution. The surface properties of all the synthesized surfactants were determined using surface tensiometry. Synthesized surfactants showed low critical micelle concentration (CMC) values and a decreasing trend with an increase in the alkyl chain length. Alkyl branching also led to a mild change in CMC values when compared with linear counterparts having the same number of carbon atoms, though such decreases or increases were observed to be dependent on the position and number of the branching. Some of the synthesized surfactants exhibited good antimicrobial and anti-cancer activities against the tested microbial strains and cell lines.