3274-34-8

Usage

Type

Synthetic pyrethroid insecticide

Applications

Agricultural and household use

Pest Control

Mosquitoes, flies, ants, cockroaches, and ticks

Mode of Action

Disrupts the nervous system of insects, leading to paralysis and death

Toxicity to Humans

Low toxicity

Toxicity to Mammals

Low toxicity

Toxicity to Aquatic Organisms

Can be toxic

Toxicity to Bees

Can be toxic

Safety Precautions

Follow safety guidelines and regulations to minimize potential harm to non-target organisms and the environment.

Upstream product

• 1165-06-6 Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 74-88-4 methyl iodide 
• 100-52-7 benzaldehyde 
• 21759-70-6 ethyl (Z)-3-(methylamino)-2-butenoate 
• 127896-76-8 N-(1-chlorobenzyl)pyridinium chloride 
• 870-85-9 ethyl 3-methylaminocrotonate 

Downstream Products

• 77548-30-2 4-methyl-2-oxo-6-phenyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 5337-88-2 3-methyl-5-phenyl-2-cyclohexen-1-one 
• 261-31-4 thioxanthene 
• 47428-55-7 3,5-Bis-ethoxycarbonyl-1,2,6-trimethyl-4-phenyl-pyridinium 
• 1352566-24-5 C₂₀H₂₃Br₂NO₄ 
• 95486-25-2 diethyl 5-methyl-3?oxo-1,2,3,6-tetrahydro-[1,1'-biphenyl]-2,6-dicarboxylate 
• 1165-06-6 Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 110531-41-4 1,2,6-trimethyl-4-phenyl-piperidine-3,5-dicarboxylic acid diethyl ester 
• 103278-83-7 2,4-bis-[1-(2,4-dinitro-phenylhydrazono)-ethyl]-3-phenyl-glutaric acid diethyl ester 

Relevant academic research and scientific papers

Metalation of Hantzsch Esters and Mixed Amide Esters: A General Route to C-2 Functionalized 1,4-Dihydropyridines

1,4-Dihydropyridine (Hantzsch) diesters 3a-e readily undergo metalation at the C-2 methyl (vinylogous ester) position on treatment with alkyllithium bases.The resulting anion intermediates can be treated with electrophilic reagents to afford 1,4-dihydropy

Novel synthese of heterocycles with N-(1-haloalkyl)azinium halides. Part 5. Preparation of N-substituted 1,4-dihydropyridines

Thirty N-substituted Hantzsch 1,4-dihydropyridines were prepared under mild and neutral conditions from N-substituted enaminocarbonyl derivatives and aldehydes activated under the form of N-(1-chloroalkyl)pyridinium chlorides by means of thionyl chloride