62574-66-7

Usage

Uses

Used in Agrochemical Industry:
Benzoyl chloride, 4-chloro-3-(chlorosulfonyl)-, is used as an intermediate in the production of agrochemicals for its ability to react with various functional groups, enabling the synthesis of a wide range of compounds with pesticidal properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, benzoyl chloride, 4-chloro-3-(chlorosulfonyl)-, is utilized as an intermediate for the synthesis of various pharmaceutical compounds, including sulfonamides, which are a class of antimicrobial agents.
Used in Organic Synthesis:
Benzoyl chloride, 4-chloro-3-(chlorosulfonyl)-, is used as a reagent in organic synthesis for its versatility in reacting with a broad spectrum of functional groups, facilitating the creation of diverse chemical compounds, including sulfones and sulfonates.

Upstream product

• 2494-79-3 4-chloro-3-(chlorosulfonyl)benzoic acid 
• 74-11-3 para-chlorobenzoic acid 
• 5216-25-1 4-chlorotrichloromethylbenzene 

Downstream Products

• 91193-68-9 2-chloro-5-(morpholine-4-carbonyl)-benzenesulfonyl chloride 
• 54208-07-0 4-(4-chloro-3-sulfamoyl-benzoyl)-morpholine 
• 90650-30-9 2-chloro-5-(dimethylcarbamoyl)benzene-1-sulfonyl chloride 

Relevant academic research and scientific papers

HEPATITIS B ANTIVIRAL AGENTS

The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: [in-line-formulae]X-A-Y-L-R??(I)[/in-line-formulae] which inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere w

Bis-Acylated Hydroxylamine Derivatives

The invention provides certain bis-acylated hydroxylamine derivative compounds, pharmaceutical compositions and kits comprising such compounds, and methods of using such compounds or pharmaceutical compositions. In particular, the invention provides methods of using such compounds or pharmaceutical compositions for treating, preventing, or delaying the onset and/or develop of a disease or condition. In some embodiments, the disease or condition is selected from cardiovascular diseases, ischemia, reperfusion injury, cancerous disease, pulmonary hypertension and conditions responsive to nitroxyl therapy.

General and Highly Efficient Syntheses of m-Fluoro Arenes Using Potassium Fluoride-Exchange Method

Tetraphenylphosphonium bromide was found to be a suitable catalyst for the reaction of m-nitroaryl derivatives carrying cyano, nitro, chlorocarbonyl, trifluoromethyl, and chlorosulfonyl groups with potassium fluoride in the presence of a stoichiometric amount of phthaloyl dichloride, giving the corresponding m-fluoro aromatic derivatives in good yields.The catalyst was also found to be efficient for the fluorodesulfonylation of m-(fluorosulfonyl)aryl derivatives to afford m-fluoro arenes by the use of a reaction-distillation technique.