63659-85-8

Usage

Uses

Used in Agricultural Industry:
3-(4-Fluoro-phenyl)-1-methyl-propylamine is used as a herbicide for controlling the growth of unwanted plants in agricultural fields. Its chemical structure allows it to target specific plant enzymes, effectively inhibiting their growth and helping to protect crops from competition and damage.
Used in Plant Growth Regulation:
In addition to its herbicidal properties, 3-(4-Fluoro-phenyl)-1-methyl-propylamine can also be used as a plant growth regulator. It can help manage and control the growth of plants, promoting healthier and more productive crops. This application can be particularly useful in optimizing agricultural practices and improving crop yields.

Upstream product

• 63416-61-5 4-(4-fluorophenyl)-2-butanone 
• 459-57-4 4-fluorobenzaldehyde 
• 65300-29-0 4-(4-fluorophenyl)but-3-en-2-one 
• 352-11-4 1-chloromethyl-4-fluorobenzene 
• 88023-07-8 ethyl 2-<(4-fluorophenyl)methyl>-3-oxobutanoate 

Downstream Products

• 63659-73-4 1-[4-(2-Cyclobutylmethoxy-ethyl)-phenoxy]-3-[3-(4-fluoro-phenyl)-1-methyl-propylamino]-propan-2-ol 

Relevant academic research and scientific papers

8-Hydroxyquinolin-2(1H)-one analogues as potential β2-agonists: Design, synthesis and activity study

β2-Agonists that bind to plasmalemmal β2-adrenoceptors causing cAMP accumulation are widely used as bronchodilators in chronic respiratory diseases. Here, we designed and synthesized a group of 8-hydroxyquinolin-2(1H)-one analogues and studied their β2-agonistic activities with a cellular cAMP assay. Compounds B05 and C08 were identified as potent (EC50 2-agonists among the compounds tested. They behaved as partial β2-agonists in non-overexpressed HEK293 cells, and possessed rapid smooth muscle relaxant actions and long duration of action in isolated guinea pig tracheal strip preparations. In summary, B05 and C08 are β2-agonists with potential applicability in chronic respiratory diseases.

Synthesis and histamine H2-agonistic activity of ring-substituted phenyl analogues of impromidine

Analogues of the H2-agonist impromidine, characterized by a substituted phenyl ring instead of the 5-methyl-4-imidazolyl group, were prepared and tested for their H2-agonistic and H1-antagonistic activity at the guinea-pig