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2-(2-chloroethoxy)-1-phenylethanol is an organic compound with the molecular formula C10H13ClO2. It is a colorless liquid with a molecular weight of 200.67 g/mol. This chemical is characterized by the presence of a phenyl group (C6H5) attached to a chiral center, which is connected to a hydroxyl group (-OH) and a 2-chloroethoxy group (-OCH2CH2Cl). The 2-chloroethoxy group is a chlorinated ether, which can potentially undergo nucleophilic substitution reactions. 2-(2-chloroethoxy)-1-phenylethanol is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. It is important to handle this substance with care due to its potential reactivity and the presence of a chlorinated group, which can pose environmental and health risks if not managed properly.

879-73-2

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879-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879-73-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 879-73:
(5*8)+(4*7)+(3*9)+(2*7)+(1*3)=112
112 % 10 = 2
So 879-73-2 is a valid CAS Registry Number.

879-73-2Relevant academic research and scientific papers

Synthesis of Substituted Dithia-9-crown-3-ethers

Romdhani, M.,Chaabouni, M. M.

, p. 3939 - 3948 (2007/10/03)

Diethylene glycol monochlorides were prepared from epoxides by action of the chloroethanol. Their conversion into substituted dithia-9-crown-3-ethers has been realized by treatment with p-toluenesulfonyl chloride, followed by the action of 1,2-dimercaptoe

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