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2-Chloroethyl 1-phenylethyl ether is an organic compound with the chemical formula C10H13ClO. It is a colorless liquid at room temperature and is soluble in most organic solvents. This ether derivative is formed by the reaction of 2-chloroethanol with 1-phenylethanol in the presence of a suitable catalyst, such as concentrated sulfuric acid. The compound is characterized by a chloroethyl group attached to an oxygen atom, which is further connected to a phenylethyl group. It is used in various chemical syntheses, particularly in the preparation of pharmaceuticals and agrochemicals, due to its reactivity and the presence of a reactive chlorine atom that can participate in substitution reactions. It is important to handle 2-chloroethyl 1-phenylethyl ether with care, as it may have potential health risks and should be stored away from heat and open flames.

1462-38-0

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1462-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1462-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1462-38:
(6*1)+(5*4)+(4*6)+(3*2)+(2*3)+(1*8)=70
70 % 10 = 0
So 1462-38-0 is a valid CAS Registry Number.

1462-38-0Downstream Products

1462-38-0Relevant articles and documents

Bronsted acid-catalyzed nucleophilic substitution of alcohols

Sanz, Roberto,Martinez, Alberto,Miguel, Delia,Alvarez-Gutierrez, Julia M.,Rodriguez, Felix

, p. 1841 - 1845 (2006)

Simple Bronsted acids such as p-toluene-sulfonic acid monohydrate (PTS) or polymer-bound p-toluenesulfonic acid efficiently catalyze the direct nucleophilic substitution of the hydroxy group of allylic and benzylic alcohols with a large variety of carbon- and heteroatom-centered nucleophiles. Reaction conditions are mild, the process is conducted under an atmosphere of air without the need for dried solvents, and water is the only side product of the reaction.

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