40897-41-4

Basic information

• Product Name: bis(3-aminophenyl)-disulfide
• Synonyms: bis(3-aminophenyl)-disulfide
• CAS NO: 40897-41-4
• Molecular Weight: 248.373
• Mol File: 40897-41-4.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: bis(3-aminophenyl)-disulfide(CAS DataBase Reference)
• NIST Chemistry Reference: bis(3-aminophenyl)-disulfide(40897-41-4)
• EPA Substance Registry System: bis(3-aminophenyl)-disulfide(40897-41-4)

Safety Data

• Hazardous Substances Data: 40897-41-4(Hazardous Substances Data)

Upstream product

• 22948-02-3 3-aminothiophenol 
• 1295576-13-4 C₆H₉N₃*ClH 
• 6655-77-2 3-nitrophenylsulfonohydrazide 
• 38045-50-0 3-nitro-benzenethiosulfonic acid S-(3-nitro-phenyl ester) 
• 121-51-7 3-nitrobenzenesulphonyl chloride 
• 537-91-7 bis(3-nitrophenyl) disulfide 
• 7705-08-0 iron(III) chloride 
• 7647-01-0 hydrogenchloride 
• 7664-93-9 sulfuric acid 

Downstream Products

• 1616689-88-3 N-[3-(3-(3-trifluoromethyl)-benzoylaminophenyldisulfanyl)-phenyl]-benzamide 
• 1616689-52-1 5-[3-(3-trifluoromethylbenzoylamino)-phenylsulfanylmethyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester 
• 1393847-33-0 1-ethoxymethyl-6-(3-aminophenylthio)thymine 
• 1393847-27-2 1-(2,5-dimethylbenzyl)-6-(3-aminophenylthio)uracil 
• 1393847-19-2 1-((2-trimethylsilylethoxy)methyl)-6-(3-aminophenylthio)uracil 
• 1188907-38-1 1-(5-tert-butylisoxazol-3-yl)-3-(3-(6,7-dimethoxyquinazolin-4-ylthio)phenyl)urea hydrochloride 
• 1188907-37-0 1-(5-tert-butylisoxazol-3-yl)-3-(3-(6,7-dimethoxyquinazolin-4-ylthio)phenyl)urea 
• 1188907-35-8 1-(5-tert-butylisoxazol-3-yl)-3-(3-mercaptophenyl)urea 
• 1188907-34-7 1,1'-(3,3'-disulfanediylbis(3,1-phenylene))bis(3-(5-tert-butylisoxazol-3-yl)urea) 
• 22948-02-3 3-aminothiophenol 
• 23905-49-9 3-thiocyanatoaniline 
• 79576-16-2 potassium 3-aminothiophenoxide 
• 52017-33-1 bis-(3-benzoylamino-phenyl)-disulfide 

Relevant articles and documents

Novel allosteric covalent inhibitors of bifunctional Cryptosporidium hominis TS-DHFR from parasitic protozoa identified by virtual screening

Protozoans of the genus Cryptosporidium are the causative agent of the gastrointestinal disease, cryptosporidiosis, which can be fatal in immunocompromised individuals. Cryptosporidium hominis (C. hominis) bifunctional thymidylate synthase-dihydrofolate r

Accelerated reduction and solubilization of elemental sulfur by 1,2-aminothiols

Nucleophilic 1,2-aminothiol compounds readily reduce typically-insoluble elemental sulfur to polysulfides in both water and nonpolar organic solvents. The resulting anionic polysulfide species are stabilized through hydrogen-bonding interactions with the proximal amine moieties. These interactions can facilitate sulfur transfer to alkenes.

Natural gallic acid catalyzed aerobic oxidative coupling with the assistance of MnCO3 for synthesis of disulfanes in water

The formation of S-S bonds has great significance and value in synthetic chemistry and bioscience. To pursue a sustainable approach for such a synthesis, an aerobic oxidative coupling method for the efficient preparation of organic disulfanes, using a low-toxic natural gallic acid as an organocatalyst, inexpensive MnCO3 as a cocatalyst, O2 as the terminal oxidant and water as the solvent, has been successfully developed. Such metal-organic cooperative catalytic protocol provided an access to various symmetrical and unsymmetrical disulfanes in up to 99% yield. Gram scale synthesis with practical convenience and low loading of catalysts further illustrates the practicability of our method.