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α,β-Dibromoethyl phenyl ether is an organic compound with the chemical formula C8H8Br2O. It is a colorless to pale yellow liquid that is insoluble in water but soluble in organic solvents. α,β-dibromoethyl phenyl ether is formed by the reaction of phenol with 1,2-dibromoethane, resulting in the formation of an ether linkage between the phenol and the dibromoethyl group. α,β-Dibromoethyl phenyl ether is used as a chemical intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. It is also known for its potential use as a reagent in organic synthesis due to its ability to participate in various chemical reactions, such as nucleophilic substitutions and eliminations. However, it is important to handle α,β-dibromoethyl phenyl ether with care due to its potential toxicity and environmental impact.

42220-93-9

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42220-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42220-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,2 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42220-93:
(7*4)+(6*2)+(5*2)+(4*2)+(3*0)+(2*9)+(1*3)=79
79 % 10 = 9
So 42220-93-9 is a valid CAS Registry Number.

42220-93-9Upstream product

42220-93-9Relevant academic research and scientific papers

Reactions of selenium dichloride and dibromide with unsaturated ethers. Annulation of 2,3-dihydro-1,4-oxaselenine to the benzene ring

Potapov, Vladimir A.,Musalov, Maxim V.,Amosova, Svetlana V.

, p. 4606 - 4610 (2011)

Highly chemo-, regio-, and stereoselective syntheses of novel organoselenium compounds from selenium dichloride or dibromide and unsaturated ethers are described. The reactions of selenium dichloride with allyl and propargyl phenyl ethers afford either annulated products or bis-adducts depending on the conditions. The first examples of annulation of 3-chloromethyl- and 3-chloromethylene-2,3-dihydro-1,4-oxaselenine to the benzene ring are reported.

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