61946-89-2

Basic information

• Product Name: (Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL
• Synonyms: (Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL
• CAS NO: 61946-89-2
• Molecular Formula: C₉H₁₀ClNO₂
• Molecular Weight: 199.63
• Mol File: 61946-89-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL(61946-89-2)
• EPA Substance Registry System: (Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL(61946-89-2)

Safety Data

• Hazardous Substances Data: 61946-89-2(Hazardous Substances Data)

Usage

Description

(Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL, also known as chlorophenothrin, is a synthetic chemical compound belonging to the pyrethroid class of insecticides. It possesses a molecular formula of C10H11ClO2 and is characterized by its effectiveness in controlling a broad spectrum of insects, such as mosquitoes, flies, and ants. Chlorophenothrin operates by disrupting the nervous system of insects, causing paralysis and ultimately death. However, it is also toxic to aquatic organisms and has raised concerns regarding its potential impact on human health and the environment. As a result, it is crucial to exercise caution and adhere to safety guidelines and regulations when handling and applying chlorophenothrin.

Uses

Used in Agricultural Applications:
(Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL is used as an insecticide for controlling various pests in agricultural settings. Its application helps protect crops from damage caused by insects, ensuring a higher yield and better quality of produce.
Used in Residential Applications:
(Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL is also used as an insecticide in residential settings to control household pests, such as mosquitoes and flies. Its effectiveness in eliminating these insects contributes to a healthier and more comfortable living environment.
Used in Environmental Management:
(Z)-2-CHLORO-2-(4-ETHOXYPHENYL)ETHENOL is employed in environmental management as a tool for controlling insect populations that may pose risks to ecosystems or human health. Its targeted application helps maintain a balance in the ecosystem while minimizing the potential negative impacts on non-target species.

Upstream product

• 10031-82-0 4-ethoxybenzaldehyde 
• 61096-94-4 4-ethoxybenzaldoxime 
• 61096-94-4 N-[(E)-(4-ethoxyphenyl)methylidene]hydroxylamine 
• 123-08-0 4-hydroxy-benzaldehyde 

Relevant articles and documents

Dibenzazepine-linked isoxazoles: New and potent class of α-glucosidase inhibitors

α-Glucosidase inhibition is a valid approach for controlling hyperglycemia in diabetes. In the current study, new molecules as a hybrid of isoxazole and dibenzazepine scaffolds were designed, based on their literature as antidiabetic agents. For this, a series of dibenzazepine-linked isoxazoles (33–54) was prepared using Nitrile oxide-Alkyne cycloaddition (NOAC) reaction, and evaluated for their α-glucosidase inhibitory activities to explore new hits for treatment of diabetes. Most of the compounds showed potent inhibitory potency against α-glucosidase (EC 3.2.1.20) enzyme (IC50 = 35.62 ± 1.48 to 333.30 ± 1.67 μM) using acarbose as a reference drug (IC50 = 875.75 ± 2.08 μM). Structure-activity relationship, kinetics and molecular docking studies of active isoxazoles were also determined to study enzyme-inhibitor interactions. Compounds 33, 40, 41, 46, 48–50, and 54 showed binding interactions with critical amino acid residues of α-glucosidase enzyme, such as Lys156, Ser157, Asp242, and Gln353.

N -Oxide-Controlled Chemoselective Reduction of Nitrofuroxans

A facile and chemoselective SnCl 2 -mediated mild reduction of regioisomeric 3- and 4-nitrofuroxans for the synthesis of aminofurazans and aminofuroxans in good yields is developed. Reduction of 4-nitrofuroxans results in the selective formation of 4-aminofuroxans, while analogous reduction of 3-nitrofuroxans affords 3-aminofurazans as a result of simultaneous reduction of the nitro group and exocyclic N-O bond.

N-(sulfonyloxy) benzimidoyl halides as bactericidal or fungicidal agents

Agricultural fungicidal compositions based on N-(sulfonyloxy)benzimidoyl halides exhibit a broad spectrum of antifungal activity, particularly against late blight, bean rust and rice blast. The synthesis of representative compounds is described, and the utility of antifungal compositions is exemplified.