53347-49-2

Usage

Uses

Used in Chemical and Engineering Processes:
2,2'-Diamino[sulfonylbisbenzene] is used as an intermediate in the synthesis of various chemical compounds and materials. Its unique structure allows it to be a versatile building block for the development of new molecules with specific properties and applications.
Used in Quality Control:
In the field of quality control, 2,2'-Diamino[sulfonylbisbenzene] is used for the preparation and analysis of diamino di-Ph sulfone. High-performance liquid chromatography (HPLC) is employed to ensure the purity and consistency of the final product, which is crucial for its performance in various applications.
Used in Pharmaceutical Industry:
2,2'-Diamino[sulfonylbisbenzene] is used as a key component in the development of pharmaceutical compounds. Its unique chemical structure allows it to be modified and functionalized to create new drugs with specific therapeutic properties.
Used in Material Science:
In material science, 2,2'-Diamino[sulfonylbisbenzene] is used as a building block for the development of new materials with tailored properties. Its incorporation into polymers and other materials can lead to improved mechanical, thermal, and chemical properties, making it suitable for various applications, such as coatings, adhesives, and composites.

Upstream product

• 127-63-9 diphenyl sulphone 
• 107411-00-7 acetic acid-[2-(2-nitro-benzenesulfonyl)-anilide] 
• 98-95-3 nitrobenzene 
• 23773-60-6 2-phenyl-2H-1,2,4-benzothiadiazine 1,1-dioxide 
• 27332-20-3 N-phenyl-2-amino-benzenesulfonamide 
• 101954-59-0 3-methyl-2-phenyl-2H-1,2,4-benzothiadiazine 1,1,-dioxide 
• 101954-71-6 N-(2'-formamidobenzenesulfonyl)aniline 
• 4273-98-7 2-aminophenyl phenyl sulfone 
• 14665-52-2 2,2'-dinitrodiphenyl sulfone 

Downstream Products

• 5194-23-0 dibenzo[1,4,5]thiadiazepine 5,11,11-trioxide 
• 100136-77-4 N-[2-(2-nitroso-benzenesulfonyl)-phenyl]-hydroxylamine 
• 5194-21-8 Dibenzo<1,4,5>thiadiazepin-11,11-dioxid 
• 95768-71-1 Bis-<2-formylamino-phenyl>-sulfon 
• 1428-17-7 Bis-<2-trifluoracetylamino-phenyl>-sulfon 

Relevant academic research and scientific papers

Inhibitors of kynureninase

The present invention provides inhibitors of kynureninase having the formula STR1 where X is CHOH, S, SO2, SO, SONH, PO2 H or PONH2, RA and RB, independently of one another, are H, a halogen, CF3

Photoinduced Ring Enlargement Reactions of 2H-1,2,4-Benzothiadiazine 1,1-Dioxides. Steady-State and Laser Flash Photolysis Studies

Ring-enlargement reactions of several 2H-1,2,4-benzothiadiazine 1,1-dioxides under photoexcitation have been studied by steady-state irradiation, product analysis, and laser flash photolysis.Irradiations in benzene or methanol gave moderate yields (14-70p

3H-Azepines and Related Systems. Part 2. The Photolyses of Aryl Azides Bearing Electron-withdrawing Substituents

The photolyses of ortho-substituted aryl azides (o-XC6H4N3 where X = CONHNH2, CONHN=CHAr, NO2, CN, CF3, SO2OMe, SO2NH2, or SO2Ph) in methanol-tetrahydrofuran solution are described.With X = CF3 or CONHN=CHAr, 3-substituted 2-methoxy-3H-azepines are products, while in other cases polymeric products, amines or mixtures of isomeric azepines are obtained.The product from the photolysis of o-azidophenyl phenyl sulphoxide (X = SOPh) is identified tentatively (n.m.r. evidence) as 7-methoxy-2-phenylsulphinyl-3H-azepine.In contrast, methyl p-azidobenzoate and p-cyanophenyl azide yield the corresponding 5-substituted 2-methoxy-3H-azepines, whereas methyl m-azidobenzoate yields only methyl 2-methoxy-3H-azepine-6-carboxylate.Irradiation of methyl o-azidobenzoate in aqueous tetrahydrofuran gives 1,3-dihydro-3-methoxycarbonyl-2H-azepin-2-one.