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Phenol, 2-chloro-4-ethoxy-, also known as 2-chloro-4-ethoxyphenol, is a chemical compound that possesses both anti-bacterial and anti-fungal properties. It is commonly used in the production of insecticides, fungicides, and herbicides, as well as in the manufacturing of pharmaceuticals and as an intermediate in the synthesis of other organic compounds. Due to its potential toxicity and irritating nature to the skin and eyes, it is important to handle Phenol, 2-chloro-4-ethoxy- with care.

344326-18-7

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344326-18-7 Usage

Uses

Used in Pesticide Industry:
Phenol, 2-chloro-4-ethoxy-, is used as an active ingredient in the production of insecticides, fungicides, and herbicides for its anti-bacterial and anti-fungal properties. This helps in controlling and preventing the growth of harmful microorganisms and pests in agricultural settings.
Used in Pharmaceutical Industry:
Phenol, 2-chloro-4-ethoxy-, is used as a raw material in the manufacturing of pharmaceuticals. Its anti-bacterial and anti-fungal properties make it a valuable component in the development of medications for treating various infections and diseases.
Used in Organic Synthesis:
Phenol, 2-chloro-4-ethoxy-, serves as an intermediate in the synthesis of other organic compounds. Its unique chemical structure allows it to be a versatile building block for creating a wide range of chemical products.
Used in Antioxidant Applications:
Phenol, 2-chloro-4-ethoxy-, has been studied for its potential use as an antioxidant. Its ability to neutralize harmful free radicals and prevent oxidative damage makes it a promising candidate for use in various industrial and consumer products.
Used in Skin Treatment Industry:
Phenol, 2-chloro-4-ethoxy-, has been investigated for its potential use in the treatment of certain skin conditions. Its anti-bacterial and anti-fungal properties may contribute to the management and improvement of skin health.

Check Digit Verification of cas no

The CAS Registry Mumber 344326-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,3,2 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 344326-18:
(8*3)+(7*4)+(6*4)+(5*3)+(4*2)+(3*6)+(2*1)+(1*8)=127
127 % 10 = 7
So 344326-18-7 is a valid CAS Registry Number.

344326-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethoxy-2-chloro-phenol

1.2 Other means of identification

Product number -
Other names 4-Aethoxy-2-chlor-phenol

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:344326-18-7 SDS

344326-18-7Relevant academic research and scientific papers

NOVEL OLEFIN DERIVATIVE

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Paragraph 0760-0761, (2015/09/28)

The object of the present invention is to provide novel compounds having ACC2 inhibiting activity. In addition, the object of the present invention is to provide a pharmaceutical composition comprising the compound. A compound of formula (I′): wherein R1 is substituted or unsubstituted aryl etc., R2 is each independently hydrogen, substituted or unsubstituted alkyl etc., R3 is each independently hydrogen, substituted or unsubstituted alkyl etc., n is an integer from 0 to 3, R12 is hydrogen, substituted or unsubstituted alkyl etc., Ring A is aromatic carbocycle or aromatic heterocycle, R9 is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl etc., m is an integer from 0 to 4, R4 and R5 is each independently hydrogen, substituted or unsubstituted alkyl etc., R6 is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl etc., R13 is hydrogen, substituted or unsubstituted alkyl etc., X5 is bond etc., R7 is hydrogen or substituted or unsubstituted alkyl, R8 is substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl etc.

Synthesis of o-chlorophenols via an unexpected nucleophilic chlorination of quinone monoketals mediated by N,N′-dimethylhydrazine dihydrochloride

Yin, Zhiwei,Zhang, Jinzhu,Wu, Jing,Green, Riana,Li, Sihan,Zheng, Shengping

supporting information, p. 2854 - 2858 (2014/05/06)

An unexpected nucleophilic chlorination of a quinone monoketal while carrying out a pyrazolidine synthesis has led to a general preparation of multisubstituted phenols. The products are obtained in good to high yields under mild conditions. The bridged pyrazolidines that were the original targets are obtained in the presence of a protic solvent. This journal is the Partner Organisations 2014.

(2R)-2-Methylchromane-2-carboxylic acids: Discovery of selective PPARα agonists as hypolipidemic agents

Koyama, Hiroo,Boueres, Julia K.,Miller, Daniel J.,Berger, Joel P.,MacNaul, Karen L.,Wang, Pei-Ran,Ippolito, Marc C.,Wright, Samuel D.,Agrawal, Arun K.,Moller, David E.,Sahoo, Soumya P.

, p. 3347 - 3351 (2007/10/03)

A SAR study was conducted on chromane-2-carboxylic acid toward selective PPARα agonisim. As a result, highly potent, and selective PPARα agonists were discovered. The optimized compound 43 exhibited robust lowering of total cholesterol levels in hamster and dog animal models.

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