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ETHYL 4-(2-CHLOROETHOXY)BENZOATE is a chemical compound belonging to the ester class of organic compounds, derived from benzoic acid. It is typically clear to pale yellow in color, has a fruity odor, and is soluble in organic solvents while being sparingly soluble in water. ETHYL 4-(2-CHLOROETHOXY)BENZOATE is recognized for its effectiveness in controlling a broad spectrum of insects and mites, making it a valuable asset in pest management.

40992-21-0

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40992-21-0 Usage

Uses

Used in Agricultural Applications:
ETHYL 4-(2-CHLOROETHOXY)BENZOATE is used as an insecticide and acaricide for controlling a wide range of insects and mites that can damage crops and reduce agricultural productivity. Its effectiveness in pest management helps protect crops and maintain their yield.
Used in Household Applications:
In household settings, ETHYL 4-(2-CHLOROETHOXY)BENZOATE is used as an insecticide to control pests such as mosquitoes, flies, and other insects that can be a nuisance or pose health risks. Its ability to target a broad spectrum of insects makes it a versatile choice for home pest control.
It is important to handle and use ETHYL 4-(2-CHLOROETHOXY)BENZOATE with caution due to its potential to cause skin and eye irritation, and it should be considered harmful if swallowed. Proper safety measures and guidelines should be followed to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 40992-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,9 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40992-21:
(7*4)+(6*0)+(5*9)+(4*9)+(3*2)+(2*2)+(1*1)=120
120 % 10 = 0
So 40992-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H13ClO3/c1-2-14-11(13)9-3-5-10(6-4-9)15-8-7-12/h3-6H,2,7-8H2,1H3

40992-21-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 4-(2-CHLOROETHOXY)BENZOATE

1.2 Other means of identification

Product number -
Other names 2-(p-Ethoxycarbonylphenoxy)-1-chloroethane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:40992-21-0 SDS

40992-21-0Relevant academic research and scientific papers

Discovery of novel benzofuran-based compounds with neuroprotective and immunomodulatory properties for Alzheimer's disease treatment

Montanari, Serena,Mahmoud, Ali Mokhtar,Pruccoli, Letizia,Rabbito, Alessandro,Naldi, Marina,Petralla, Sabrina,Moraleda, Ignacio,Bartolini, Manuela,Monti, Barbara,Iriepa, Isabel,Belluti, Federica,Gobbi, Silvia,Di Marzo, Vincenzo,Bisi, Alessandra,Tarozzi, Andrea,Ligresti, Alessia,Rampa, Angela

, p. 243 - 258 (2019/06/14)

To address the multifactorial nature of Alzheimer's Disease (AD), a multi-target-directed ligand approach was herein developed. As a follow-up of our previous studies, a small library of newly designed 2-arylbenzofuran derivatives was evaluated towards ch

Arylalkylheterocyclic amines,N-substituted by aryloxyalkyl group in a method for allergy treatment

-

, (2008/06/13)

A method of inhibiting Type 1 allergic responses in a living animal body with substituted heterocyclic amines is disclosed wherein the active agents are expressed generally by the formula which includes certain known and certain known compounds: STR1 wherein P is zero, one or two; m is one to six inclusive; A is selected from hydrogen, hydroxy or cyano; d is zero or one; Q is --CH--, CH2 -- or STR2 n is zero or one and when Q is --CH-- and n is one, a double bond is formed with one of the adjacent carbons but not both at the same time, and when n and d are zero at the same time, a double bond is formed between the α carbon and a carbon of the central heterocyclic amine ring; Ar, D and R are selected from phenyl, substituted phenyl, pyridinyl, thienyl, furanyl or naphthyl and in addition, R may have the values benzyl, substituted benzyl, cycloalkyl or loweralkyl and D may additionally have the values: 2H-1-benzopyran-2-one,4-oxo-4H-1-benzopyran-2-carboxylic acid loweralkyl ester, 2,3-dihydro-4H-1-benzopyran-4-one, 1,4-benzodioxanloweralkyl-2-yl or 1,1'-biphenyl-4-yl and the pharmaceutically acceptable salts thereof.

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