38025-93-3

Usage

Uses

Used in Pharmaceutical Industry:
3-Pyridinesulfonamide,2-chloro-(9CI) is used as an intermediate in the synthesis of various pharmaceutical products for its potential biological and pharmacological properties, including antimicrobial and antitumor activities.
Used in Agrochemical Industry:
3-Pyridinesulfonamide,2-chloro-(9CI) is used as an intermediate in the synthesis of agrochemical products, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Organic Synthesis:
3-Pyridinesulfonamide,2-chloro-(9CI) is used as a building block in organic synthesis, enabling the creation of new compounds with potential applications in various fields.
Used as a Chemical Reagent:
3-Pyridinesulfonamide,2-chloro-(9CI) is utilized as a reagent in various chemical reactions, facilitating the synthesis of different organic compounds and contributing to the advancement of chemical research.

Upstream product

• 6298-19-7 2-chloro-3-aminopyridine 
• 6684-06-6 2-chloro-3-pyridinesulfonyl chloride 
• 6602-56-8 2-chloropyridine-3-sulfonic acid 

Downstream Products

• 84881-80-1 2-(2-Chloro-phenylsulfanyl)-pyridine-3-sulfonic acid amide 
• 84881-74-3 2-m-Tolylsulfanyl-pyridine-3-sulfonic acid amide 
• 84881-84-5 2-(3-Chloro-phenylsulfanyl)-pyridine-3-sulfonic acid amide 
• 84897-02-9 2-(3-Trifluoromethyl-phenylsulfanyl)-pyridine-3-sulfonic acid amide 
• 84881-98-1 2-(3,5-Dichloro-phenylsulfanyl)-pyridine-3-sulfonic acid amide 
• 84881-95-8 2-(3,4-Dichloro-phenylsulfanyl)-pyridine-3-sulfonic acid amide 
• 84881-92-5 2-(2,6-Dichloro-phenylsulfanyl)-pyridine-3-sulfonic acid amide 
• 84881-77-6 2-p-Tolylsulfanyl-pyridine-3-sulfonic acid amide 
• 84881-87-8 2-(4-Chloro-phenylsulfanyl)-pyridine-3-sulfonic acid amide 
• 54136-36-6 2-aminopyridine-3-sulfonamide 
• 74186-29-1 2-Hydrazino-3-aminosulfonylpyridine 
• 38030-49-8 2-(4-methyl-piperazin-1-yl)-pyridine-3-sulfonic acid amide 
• 90811-04-4 2-phenoxy-3-pyridylsulfonamide 

Relevant academic research and scientific papers

FUSED [1,2,4]THIADIAZINE DERIVATIVES WHICH ACT AS KAT INHIBITORS OF THE MYST FAMILY

A compound of formula (I): which inhibits the activity of one or more KATs of the MYST family, i.e., TIP60, KAT6B, MOZ, HBO1 and MOF.

Positive allosteric modulators of 2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic acid receptors belonging to 4-cyclopropyl-3,4-dihydro-2 H -1,2,4-pyridothiadiazine dioxides and diversely chloro-substituted 4-cyclopropyl-3,4-dihydro-2 H -1,2,4-benzot

Two 4-ethyl-substituted pyridothiadiazine dioxides belonging to α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor positive allosteric modulators were cocrystallized with the GluA2 ligand binding domain in order to decipher the impact of

Herbicidal ortho-heterocyclic sulfonamides

Herbicidally active pyridinesulfonamide compounds having an ortho cyclic saturated or partially saturated group which includes a carbonyl or sulfonyl radical display utility as herbicides and plant growth regulants.

Studies on Anticoccidial Agents. 13. Synthesis and Anticoccidial Activity of Nitropyridine-2- and -3-sulfonamides and Derivatives

Eight nitropyridinesulfonamides andd pyridinesulfonamide N-oxides as their bioisosteres were prepared and evaluated for anticoccidial activity.Of these compounds, 2-, 4- and 5-nitropyridine-3-sulfonamides and pyridine-2- and -3-sulfonamide N-oxides were found to be active against Eimeria tenella.Thus, the relative positions, ortho or meta, of the substituents in nitropyridine-3-sulfonamides and pyridinesulfonamide N-oxides are important for anticoccidial activity.N-Substituted analogues of 5-nitropyridine-3-sulfonamide were also prepared and optimal anticoccidial activity was attained with the sulfonamide and its lower N-alkyl derivatives.The mode of action of 5-nitropyridine-3-sulfonamide was examined and found to be active in the sporozoite and the first schizogony stages.

C-Piperazino-pyridine sulfonamides

This invention relates to compounds of the formula: SPC1 Wherein R1 in the 3- or 5-position is preferably a substituted sulfonamido or a carboxamido group whereas R2 in the 2-, 4- or 6-position is preferably an alkyl- or hydroxyalkyl-piperazinyl group. Said compounds may be used as anti-inflammatory and cardiovascular agents.