6579-54-0

Usage

Uses

Used in Organic Synthesis:
2,6-Dichlorobenzenesulfonyl chloride serves as a key intermediate in organic synthesis, where it is utilized for the preparation of various organic compounds. Its reactivity allows for the formation of new chemical bonds and the synthesis of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,6-dichlorobenzenesulfonyl chloride is employed as a building block for the development of new drugs. Its unique structure and functional groups enable the creation of novel pharmaceutical agents with potential therapeutic applications.
Used in Agrochemicals:
2,6-Dichlorobenzenesulfonyl chloride is used as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its properties contribute to the effectiveness of these products in controlling pests and promoting crop growth.
Used in Dye Industry:
In the dye industry, 2,6-dichlorobenzenesulfonyl chloride is utilized for the synthesis of various dyes and pigments. Its chemical structure allows for the development of dyes with specific color properties and stability, catering to the needs of different applications.

InChI:InChI=1/C6H3Cl3O2S/c7-4-2-1-3-5(8)6(4)12(9,10)11/h1-3H

Upstream product

• 24966-39-0 2,6-dichlorothiophenol 
• 7446-09-5 sulfur dioxide 
• 608-31-1 2,6-Dichloroaniline 

Downstream Products

• 24966-39-0 2,6-dichlorothiophenol 
• 4184-39-8 1,3-dichloro-2-[(2,6-dichlorophenyl)disulfanyl]benzene 
• 887903-73-3 2-(2,6-dichloro-benzenesulfonyl)-2-aza-bicyclo[2.2.2]octane-3-carboxylic acid ethyl ester 
• 6697-96-7 o-dichlorobenzenesulfonic acid 
• 376349-79-0 2,6-Dichloro-N-[4-(3-chloro-thien-2-yl)-1,3-thiazol-2-yl]benzenesulfonamide 
• 276702-52-4 2,6-dichloro-3-nitrobenzenesulfonic acid 
• 219713-14-1 2,6-dichloro-N-(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide 
• 219713-11-8 2,6-dichloro-N-(5-methoxy-1,2,4-triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide 
• 219713-20-9 2,6-dichloro-N-(8-ethoxy-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide 
• 219713-24-3 2,6-dichloro-N-(8-chloro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide 
• 219713-12-9 2,6-dichloro-N-(8-fluoro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide 
• 219713-23-2 2,6-dichloro-N-(5-methoxy-8-methyl-1,2,4-triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide 
• 1138323-43-9 2,6-dichloro-N-(7-fluoro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide 
• 1165803-16-6 C₁₃H₈Cl₂N₂O₂S 

Relevant academic research and scientific papers

Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists

The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.

Il-8 receptor antagonists

This invention relates to novel compounds of Formula (I) to (VII), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).

Il-8 receptor antagonists

This invention relates to novel compounds of Formula (I) to (VII), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).

Il-8 receptor antagonists

This invention relates to novel compounds of Formula (I) to (VII), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).

Il-8 receptor antagonists

This invention relates to novel compounds of Formula (I) to (VII), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).

1-carbonyl-2-pyrazoline derivatives having herbicidal activity

The invention relates to a herbicidally active compound of the general STR1 wherein R1, R2 R3 and R4 are equal or different and represent hydrogen atoms, alkyl groups having 1-6 carbon atoms, cycloalkyl groups having 3-6 carbon atoms or alkoxycarbonyl groups having 2-5 carbon atoms; R5 is a hydrogen atom, an alkyl group or haloalkyl group having 1-8 carbon atoms, a substituted or non-substituted phenyl group, a substituted or non-substituted heterocyclic group, or an alkenyl, alkynyl or alkoxycarbonyl group having 2-5 carbon atoms; and wherein two of the groups R1, R2, R3, R4 and R5 together may form a straight or branched alkylene group having 3-5 carbon atoms; Ar is a phenyl group, a phenyl (C1 -C4)alkyl group or a heteroaryl group; R6 is a hydrogen atom or substitutent to Ar, which substituent, in case Ar is a phenyl or phenylalkyl group, is attached to the phenyl group in the ortho position with respect to the sulphonyl or sulphonylalkyl group, and which substituent is selected from the following atoms and groups: a halogen atom; a nitro group; an alkoxycarbonyl group that has 2-8 carbon atoms and is unsubstituted or substituted with one or more hydroxy or C1 -C4 alkoxy groups; and an alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulphonyl and haloalkylsulphonyl group having 1-6 carbon atoms; and R7 represent a hydrogen atom or one or two halogen atoms or C1 -C4 alkyl groups.