41197-29-9

Usage

Uses

Used in Pharmaceutical Production:
DICHLOROMETHANESULFONYL CHLORIDE is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Production:
In the agrochemical industry, DICHLOROMETHANESULFONYL CHLORIDE is utilized as an intermediate, playing a role in the creation of compounds that protect crops and enhance agricultural productivity.
Used in Dye Production:
DICHLOROMETHANESULFONYL CHLORIDE is also employed as an intermediate in the production of dyes, which are essential for coloring textiles, plastics, and other materials.
Used as a Reagent in Organic Synthesis:
DICHLOROMETHANESULFONYL CHLORIDE is used as a reagent in organic synthesis, facilitating a variety of chemical reactions that are crucial for the synthesis of complex organic molecules.
Used as a Chlorinating Agent:
Due to its high reactivity, DICHLOROMETHANESULFONYL CHLORIDE is used as a chlorinating agent in various chemical reactions, enabling the introduction of chlorine atoms into different chemical structures for diverse applications.

InChI:InChI=1/CHCl3O2S/c2-1(3)7(4,5)6/h1H

Upstream product

• 53638-45-2 dichloro-methanesulfonic acid 
• 60812-39-7 Dichlormethandisulfonyldichlorid 
• 68-11-1 mercaptoacetic acid 

Downstream Products

• 34070-24-1 Dichlormethansulfonsaeure-<4-chlor-anilid> 
• 114304-57-3 4-Chlor-N_.N-bis-dichlormethansulfonyl-anilin 
• 101421-30-1 Dichlormethansulfonsaeure-<2.4.5-trichlor-anilid> 
• 152342-77-3 N-methyl-N-dihloromethanesulphonyl-p-hydroxybenzene 
• 25004-95-9 trichloromethanesulfinyl chloride 
• 14843-83-5 Trimethylammonium-(methylsulfonyl)methansulfonat 
• 1554-47-8 difluoromethanesulfonyl fluoride 
• 73082-92-5 4,4-Dichlor-3-phenyl-but-1-en 

Relevant academic research and scientific papers

Studies on anti-amoebic compounds. Part V. Synthesis of dichloromethanesulphonamides

Synthesis of a variety of dichloromethanesulphonamides, including a close structural analogue of a well-known drug, namely diloxanide furoate, and their anti-amoebic activities are reported. anti-amoebic compounds / diloxanide furoate / dichloroacetamides / dichloromethanesulphonamides

Experiments Concerning the Reduction of Dichloromethanedisulfonyl Dichloride

Mild reducing agents, including methanol, reduce dichloromethanedisulfonyl dichloride (2) to give dichloro(chlorosulfonyl)methanesulfinic acid (6) which desulfinylates spontaneously to form dichloromethanesulfonyl chloride (9).Chloromethanedisulfonyl dichloride (12) is not reduced under these conditions and can be derivatized "normally", for instance with morpholine.

N-sulfonyl-N-dihalophenylimidazolidinediones

3-(3' -Dihalophenyl)-1-sulfonylimidazolidine-2,4-5'-diones of the formula: STR1 wherein X is a halogen atom, R1 is a C1 -C12 alkyl group, a C2 -C4 alkenyl group or a halogenated C1 -C4 alkyl group having 1 to 3 halogen atoms, and R2 and R3 are individually a hydrogen atom or a methyl group, which show high microbicidal activities against various fungi and bacteria without any material toxicity to mammals and which plants and can be produced by reacting the corresponding 1-unsubstituted compound with a sulfonyl halide.