21731-56-6

Usage

Uses

Used in Chemical Synthesis:
4-Mesyl-2-nitroaniline is used as a chemical intermediate for the synthesis of various organic compounds. Its unique combination of functional groups allows for a wide range of reactions, making it a valuable building block in the preparation of pharmaceuticals, dyes, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-mesyl-2-nitroaniline is used as a key intermediate in the synthesis of certain drugs. Its reactivity and functional groups enable the creation of complex molecular structures that can be tailored for specific therapeutic applications.
Used in Dye Manufacturing:
4-Mesyl-2-nitroaniline is used as a precursor in the production of dyes. Its chemical properties allow for the development of dyes with unique color characteristics and stability, which are essential in various industries such as textiles, plastics, and printing.
Used in Research and Development:
In academic and industrial research settings, 4-mesyl-2-nitroaniline is used as a model compound to study reaction mechanisms and explore new synthetic pathways. Its versatility in undergoing various chemical transformations makes it an important tool for advancing the understanding of organic chemistry.

InChI:InChI=1/C7H8N2O4S/c1-14(12,13)5-2-3-6(8)7(4-5)9(10)11/h2-4H,8H2,1H3

Upstream product

• 23153-09-5 1-amino-4-methylthio-2-nitrobenzene 
• 20945-69-1 4-methanesulfonyl-1-methoxy-2-nitro-benzene 
• 22821-80-3 N-(4-methanesulfonylphenyl)acetamide 
• 60854-81-1 2-chloro-4-(methylsulfonyl)-1-nitrobenzene 
• 453-72-5 1-fluoro-4-methanesulfonyl-2-nitrobenzene 
• 97-07-4 1-chloro-4-methanesulfonyl-2-nitrobenzene 
• 54029-50-4 acetic acid-(4-methanesulfonyl-2-nitro-anilide) 

Downstream Products

• 2976-32-1 1-methanesulfonyl-3-nitro-benzene 
• 1192251-78-7 6-(methylsulfonyl)-2-(2-phenylpyrimidin-5-yl)-1H-benzimidazole 
• 1192251-77-6 6-(methylsulfonyl)-2-(6-phenylpyridazin-3-yl)-1H-benzimidazole 
• 1192251-88-9 {4-[6-(methylsulfonyl)-1H-benzimidazol-2-yl]phenyl}boronic acid 
• 1192251-64-1 6-(methylsulfonyl)-2-[4-(2-thienyl)phenyl]-1H-benzimidazole 
• 1192251-51-6 2-biphenyl-4-yl-6-(methylsulfonyl)-1H-benzimidazole 
• 1192251-87-8 2-(4-bromophenyl)-6-(methylsulfonyl)-1H-benzimidazole 
• 21731-57-7 5-methylsulphonyl-1,2-phenylenediamine 
• 20951-32-0 5-Methanesulfonyl-2-methylsulfanyl-phenylamine 
• 20945-67-9 4-Methanesulfonyl-1-methylsulfanyl-2-nitro-benzene 
• 97-10-9 2-nitro-4-methylsulphonyl-phenol 

Relevant academic research and scientific papers

NOVEL SUBSTITUTED HETEROAROMATIC COMPOUNDS AS INHIBITORS OF STEAROYL-COENZYME A DELTA-9 DESATURASE

Substituted heteroaromatic compounds of structural formula I are inhibitors of stearoyl-coenzyme A delta-9 desaturase. The compounds of the present invention are useful for the prevention and treatment of conditions related to abnormal lipid synthesis and metabolism, including cardiovascular disease, such as atherosclerosis; obesity; Type 2 diabetes; insulin resistance; hyperglycemia; Metabolic Syndrome; neurological disease; cancer; and liver steatosis. Formula (I).

Substituted (alkoxycarbonylthioureido)-(acylamino)-benzene derivatives

Benzene derivatives of the formula: STR1 wherein R1 represents alkyl, R2 represents a group --SR3, --SOR3, --SO2 R3, --OR3, --SCONH2, --SCN or --T(CH2)m T1 R4 [wherein R3 represeents alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, unsubstituted or substituted aryl, or cycloalkylalkyl, R4 represents hydrogen or alkyl, T and T1 each represent oxygen, sulphur or sulphinyl, and m is an integer from 1 to 7] whose position on the benzene ring is either para to the group --NHCSNHCOOR1 or para to the group --NHCOAZ, A represents a bivalent straight-chain aliphatic hydrocarbon radical of 1 to 4 carbon atoms or a said hydrocarbon radical substituted by at least one methyl group, and Z represents a group of the formula:- STR2 wherein R5 represents hydrogen or alkyl, R6 represents hydrogen, alkyl or phenylalkyl, and R7 represents hydrogen or alkyl, or R6 and R7 together with the nitrogen atom to which they are attached form a 5-,6- or 7-membered heterocyclic ring optionally substituted by alkyl group(s), and X- represents a pharmaceutically acceptable anion, are new compounds useful as anthelmintics and antifungal agents.

Substituted 1-sulfonylbenzimidazoles

Certain 1-sulfonyl-2,5(6)-substituted-benzimidazole compounds are useful as antiviral agents.