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2-(2,6-dichlorophenyl)-1,3-dioxolane is an organic compound with the molecular formula C8H6Cl2O2. It features a dioxolane ring, which is a five-membered ring containing two oxygen atoms, and a 2,6-dichlorophenyl group attached to the 2-position of the dioxolane. This chemical is known for its potential use as an intermediate in the synthesis of various agrochemicals and pharmaceuticals, particularly those with insecticidal and herbicidal properties. Due to its chlorine atoms, it may also exhibit biocidal activity, making it a compound of interest in the development of new pesticides and other chemical products.

82073-58-3

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82073-58-3 Usage

Type of Compound

Nonsteroidal anti-inflammatory drug (NSAID)

Purpose

Treatment of inflammatory conditions (e.g., arthritis, pain)

Mechanism of Action

Inhibition of prostaglandin production

Prostaglandin Role

Promotion of inflammation, pain, and fever

Properties

Potent analgesic, anti-inflammatory, and antipyretic effects

Effectiveness

Reduction of pain and discomfort in inflammatory diseases

Side Effects

Gastrointestinal irritation, renal toxicity, and cardiovascular risks

Precaution

Use with caution and under supervision of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 82073-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,7 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82073-58:
(7*8)+(6*2)+(5*0)+(4*7)+(3*3)+(2*5)+(1*8)=123
123 % 10 = 3
So 82073-58-3 is a valid CAS Registry Number.

82073-58-3Relevant academic research and scientific papers

Alcohol Etherification via Alkoxy Radicals Generated by Visible-Light Photoredox Catalysis

Rivero, Alexandra R.,Fodran, Peter,Ondrejková, Alica,Wallentin, Carl-Johan

supporting information, p. 8436 - 8440 (2020/11/03)

A mechanistically divergent method is described that, employing a commercially available hypervalent iodine(III) reagent, generates alkoxy radicals from 1°, 2°, and 3° alcohols and allows their use in the functionalization of C(sp3)-H and C(sp2)-H bonds. This visible-light photoredox catalysis produces alkyl ethers via 1,5/6-hydrogen atom transfer or aryl ethers via 1,5-addition. This mild methodology provides a practical strategy for the synthesis of acetals, orthoesters, tetrahydrofurans, and chromanes.

Phosphonium salts and aldehydes from the convenient, anhydrous reaction of aryl acetals and triphenylphosphine hydrobromide

Ramanathan, Mani,Hou, Duen-Ren

, p. 98 - 108 (2013/05/09)

The reactions of aryl acetals/ketals and triphenylphosphine hydrobromide gave the corresponding aldehydes/ketones and alkyl phosphonium bromides. This reaction was applied to convert acetals/ketals to the corresponding aldehydes/ketones under an anhydrous

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