3-fluorosulphonylbenzenesulphonyl chloride

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1.What is the 3-fluorosulphonylbenzenesulphonyl chloride ?

3-fluorosulphonylbenzenesulphonyl chloride is an organofluorine chemical compound with the molecular formula C6H4ClFO4S2. It is a sulfonyl chloride, characterized by a functional group with a sulfur atom bonded to two oxygen atoms and a chlorine atom. 3-fluorosulphonylbenzenesulphonyl chloride is recognized for its high reactivity and serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and other chemical products.

2.What is the CAS number for 3-fluorosulphonylbenzenesulphonyl chloride ?

The CAS number of 3-fluorosulphonylbenzenesulphonyl chloride is 2489-52-3.

3.What are another words for 3-fluorosulphonylbenzenesulphonyl chloride ?

Synonyms?for?3-fluorosulphonylbenzenesulphonyl chloride 2489-52-3:m-Benzenedisulfonylchloride fluoride (7CI,8CI); 3-(Fluorosulfonyl)benzenesulfonyl chloride; NSC310025; m-(Fluorosulfonyl)benzenesulfonyl chloride

4.What is 3-fluorosulphonylbenzenesulphonyl chloride (2489-52-3) used for?

Used in Pharmaceutical Industry:
3-fluorosulphonylbenzenesulphonyl chloride is used as a key intermediate for the synthesis of various pharmaceuticals. Its reactivity allows for the creation of a wide range of organic compounds through nucleophilic substitution reactions, which are vital in developing new drugs and improving existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, 3-fluorosulphonylbenzenesulphonyl chloride is utilized as a building block in the development of pesticides and other agricultural chemicals. Its role in organic synthesis contributes to the production of effective and targeted agrochemicals that aim to enhance crop protection and yield.
Used in Organic Synthesis:
3-fluorosulphonylbenzenesulphonyl chloride is employed as a reactive building block in organic synthesis across various chemical industries. Its ability to participate in nucleophilic substitution reactions makes it a valuable component in creating diverse organic compounds for different applications, including specialty chemicals and materials.
It is important to handle 3-fluorosulphonylbenzenesulphonyl chloride with care due to its potential reactivity and toxicity, ensuring safety measures are in place throughout its use in research and industrial applications.

InChI:InChI=1/C6H4ClFO4S2/c7-13(9,10)5-2-1-3-6(4-5)14(8,11)12/h1-4H

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