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4-(2-chloroethoxy)phenol, also known as cephaeline, is a synthetic chemical compound with the molecular formula C8H9ClO2. It is a phenolic compound that contains a chlorine atom and an ethoxy group attached to a phenol ring. This colorless to light yellow liquid with a slightly phenolic odor is commonly used in the production of various pharmaceuticals and agrochemicals due to its antimicrobial and antibacterial properties. It also serves as an intermediate in the synthesis of other organic compounds. Proper safety precautions are necessary when handling 4-(2-chloroethoxy)phenol, as it can irritate the skin, eyes, and respiratory system.

100238-55-9

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100238-55-9 Usage

Uses

Used in Pharmaceutical Industry:
4-(2-chloroethoxy)phenol is used as an active ingredient for its antimicrobial and antibacterial properties, contributing to the development of various pharmaceutical products.
Used in Agrochemical Industry:
4-(2-chloroethoxy)phenol is used as a component in agrochemicals to provide protection against microbial and bacterial infections in crops, ensuring better yield and quality.
Used as an Intermediate in Organic Synthesis:
4-(2-chloroethoxy)phenol is used as a key intermediate in the synthesis of other organic compounds, facilitating the creation of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 100238-55-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,3 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100238-55:
(8*1)+(7*0)+(6*0)+(5*2)+(4*3)+(3*8)+(2*5)+(1*5)=69
69 % 10 = 9
So 100238-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClO2/c9-5-6-11-8-3-1-7(10)2-4-8/h1-4,10H,5-6H2

100238-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-CHLOROETHOXY)PHENOL

1.2 Other means of identification

Product number -
Other names Phenol,4-(2-chloroethoxy)

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:100238-55-9 SDS

100238-55-9Relevant academic research and scientific papers

An efficient multigram-scale synthesis of 4-(ω-chloroalkoxy)phenols

Zinin,Stepanova,Jost,Kondakov,Shpirt,Chizhov,Torgov,Kononov

, p. 304 - 312 (2017/07/11)

Efficient multigram two-step syntheses of 4-(2-chloroethoxy)phenol and 4-(3-chloropropoxy)phenol in >70% yields starting from 4-hydroxybenzaldehyde and reagents with general formula Cl(CH2)nX (X = Cl, n = 2; X = OTs, n = 3) are proposed. 4-(2-Chloroethoxy)phenol can also be conveniently prepared from 4-methoxyphenol and 1,2-dichloroethane. The compounds thus obtained can be used in carbohydrate chemistry to synthesize glycosides bearing "universal" 4-(ω-chloroalkoxy)phenyl aglycons.

General method for the synthesis of salicylic acids from phenols through palladium-catalyzed silanol-directed C-H carboxylation

Wang, Yang,Gevorgyan, Vladimir

supporting information, p. 2255 - 2259 (2015/02/19)

A silanol-directed, palladium-catalyzed C-H carboxylation reaction of phenols to give salicylic acids has been developed. This method features high efficiency and selectivity, and excellent functional-group tolerance. The generality of this method was demonstrated by the carboxylation of estrone and by the synthesis of an unsymmetrically o,o′-disubstituted phenolic compound through two sequential C-H functionalization processes.

One step hair coloring compositions using salts

-

, (2008/06/13)

A hair coloring composition comprising the following two compositions which are mixed just prior to application to the hair: (a) a composition comprising a water-soluble peroxygen oxidizing agent; and (b) a composition comprising one or more oxidative hair coloring agents selected from the group consisting of an aromatic diamine, an amino phenol, a naphthol, a polyhydric phenol, a catechol and mixtures thereof; wherein the composition comprising one or more oxidative hair coloring agents further comprises al least one water soluble carbonate releasing salts; and optionally a water soluble ammonium salt, is described.

Transition metal complexes as dye forming catalysts in hair coloring compositions

-

, (2008/06/13)

A hair coloring composition comprising a first composition which comprises: (a) a dye forming transition metal salt or complex; which is first applied to the hair; and a second composition which comprises the following two compositions which are mixed just prior to application to the hair: (a) a composition comprising a water-soluble peroxygen oxidizing agent; and (b) a composition comprising one or more oxidative hair coloring agents selected from the group consisting of an aromatic diamine, an aminophenol, a polyhydric phenol a catechol and mixtures thereof.

Enhanced color deposition for hair with sequestering agents

-

, (2008/06/13)

Hair coloring compositions which comprise: (A) non-nitrogenous chelating agents from the group consisting of polyphosphate; phosphonates; hydroxycarboxylates; polyacrylates; zeolite; and mixtures thereof; (B) an oxidative dye primary intermediate; and (C) an oxidative dye coupler; (D) and water are described. The present invention also relates to a method for coloring hair which comprises contacting said hair with a hair coloring composition as described above.

Chiral basket-shaped host compounds derived from diphenylglycoluril

Coolen, H. K. A. C.,Engelkamp, H.,Reek, J. N. H.,Priem, A. H.,Leeuwen, P. W. N. M. van,Nolte, R. J. M.

, p. 65 - 72 (2007/10/02)

The design and synthesis of two novel chiral receptors derived from diphenylglycoluril are described.The chirality in these molecules is due to the unsymmetrical positioning of amino functions in the crown ether rings with respect to the diphenylglycoluri

Enzyme-activated oxidative process for coloring hair

-

, (2008/06/13)

An enzyme-based oxidative process for coloring hair wherein the hair is exposed to a solution having a pH of about 4 to about 10 and containing hydrogen peroxide, soybean peroxidase enzyme and one or more oxidation dye precursors.

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