473-42-7

Usage

Uses

Used in Pharmaceutical Industry:
Nitrosulfathiazole is used as an antibiotic agent for treating bacterial infections. It works by inhibiting the synthesis of bacterial cell walls, leading to the death of the bacteria.
Used in Veterinary Medicine:
In the veterinary industry, Nitrosulfathiazole is used as a growth promoter in livestock. It helps in improving the overall health and growth of animals by preventing bacterial infections.
Used in Food Preservation:
Nitrosulfathiazole is also used as a preservative in the food industry. It helps in preventing the growth of bacteria and other microorganisms, thereby extending the shelf life of food products.
Used in Cosmetics Industry:
In the cosmetics industry, Nitrosulfathiazole is used as a preservative in various cosmetic products. It helps in maintaining the freshness and quality of the products by preventing microbial contamination.
Used in Textile Industry:
Nitrosulfathiazole is used in the textile industry as a dye fixative. It helps in improving the colorfastness and durability of dyed fabrics by forming a protective layer around the fibers.
Used in Water Treatment:
In the water treatment industry, Nitrosulfathiazole is used as a disinfectant. It helps in killing bacteria and other harmful microorganisms present in water, ensuring the safety and quality of drinking water.

InChI:InChI=1/C9H7N3O4S2/c13-12(14)7-1-3-8(4-2-7)18(15,16)11-9-10-5-6-17-9/h1-6H,(H,10,11)

Upstream product

• 96-50-4 2-thiazolylamine 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 13088-17-0 4-nitro-benzenesulfinyl chloride 

Downstream Products

• 858500-74-0 4-nitro-benzenesulfonic acid-(methyl-thiazol-2-yl-amide) 
• 72-14-0 Sulfathiazole 
• 14945-47-2 4-nitro-N-(3-xanthen-9-yl-3H-thiazol-2-ylidene)-benzenesulfonamide 
• 935266-70-9 N-{1-methyl-3-[2-(4-phenoxy-phenoxy)-thiazol-5-yl]-prop-2-ynyl}-4-nitro-N-thiazol-2-yl-benzenesulfonamide 

Relevant academic research and scientific papers

3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.

In vitro and in vivo antileishmanial and trypanocidal studies of new N -benzene- and N -naphthalenesulfonamide derivatives

We report in vivo and in vitro antileishmanial and trypanocidal activities of a new series of N-substituted benzene and naphthalenesulfonamides 1-15. Compounds 1-15 were screened in vitro against Leishmania infantum, Leishmania braziliensis, Leishmania gu

In vivo and in vitro anti-leishmanial activities of 4-nitro-N-pyrimidinand N-pyrazin-2-ylbenzenesulfonamides, and N2-(4-nitrophenyl)-N 1propylglycinamide

A series of compounds containing the nitrobenzene and sulfonamido moieties were synthesized and their leishmanicidal effect was assessed in vitro against Leishmania infantum promastigotes. Among the compounds evaluated, the p-nitrobenzenesulfonamides 4Aa

PYRIMIDINE SULFONAMIDE ANALOGS AND THEIR USE AS AGONISTS OF THE WNT-BETA-CATENIN CELLULAR MESSAGING SYSTEM

The present invention relates to pyrimidine sulfonamide analogs, methods of making pyrimidine sulfonamide analogs, compositions comprising a pyrimidine sulfonamide analog, and methods for treating canonical Wnt-β-catenin cellular messaging system-related disorders comprising administering to a subject in need thereof an effective amount of a pyrimidine sulfonamide analog.

The synthesis and structure-activity relationship studies of selective acetyl-CoA carboxylase inhibitors containing 4-(thiazol-5-yl)but-3-yn-2-amino motif: Polar region modifications

The structure-activity relationship study focused on the polar region of the HTS hit A-80040 (1) producing several series of potent and selective ACC2 inhibitors. The SAR suggests a compact lipophilic pocket that does not tolerate polar and ionic groups.