1803-24-3

Usage

Uses

Used in Research and Development:
[[(diphenylcarbamothioyl)disulfanyl]carbothioyl(phenyl)amino]benzene is used as a research compound for studying the behavior and interactions of organic molecules. Its complex structure and potential reactivity make it valuable for understanding the properties and reactions of similar compounds in various scientific and industrial processes.
Used in Chemical Synthesis:
[[(diphenylcarbamothioyl)disulfanyl]carbothioyl(phenyl)amino]benzene is used as a chemical intermediate in the synthesis of other organic compounds. Its unique functional groups can be utilized in various chemical reactions to produce a range of products with different applications in various industries.
Used in Pharmaceutical Industry:
[[(diphenylcarbamothioyl)disulfanyl]carbothioyl(phenyl)amino]benzene is used as a potential pharmaceutical candidate for the development of new drugs. Its unique structure and properties may offer novel therapeutic opportunities and contribute to the advancement of medicine.
Used in Material Science:
[[(diphenylcarbamothioyl)disulfanyl]carbothioyl(phenyl)amino]benzene is used in material science for the development of new materials with specific properties. Its unique structure and functional groups can be exploited to create materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials for electronics and energy storage.

Upstream product

• 75-15-0 carbon disulfide 
• 122-39-4 diphenylamine 
• 110-86-1 pyridine 
• 7553-56-2 iodine 
• 2801-05-0 sodium N,N-diphenyldithiocarbamate 
• 506-68-3 bromocyane 

Relevant academic research and scientific papers

Photoorganocatalyzed Reversible-Deactivation Alternating Copolymerization of Chlorotrifluoroethylene and Vinyl Ethers under Ambient Conditions: Facile Access to Main-Chain Fluorinated Copolymers

Fluoropolymers have found broad applications for many decades. Considerable efforts have focused on expanding access toward main-chain fluorinated polymers. In contrast to previous polymerizations of gaseous fluoroethylenes conducted at elevated temperatures and with high-pressure metallic vessels, we here report the development of a photoorganocatalyzed reversible-deactivation radical alternating copolymerization of chlorotrifluoroethylene (CTFE) and vinyl ethers (VEs) at room temperature and ambient pressure by exposing to LED light irradiation. This method enables the synthesis of various fluorinated alternating copolymers with low ? and high chain-end fidelity, allowing an iterative switch of the copolymerization between ON and OFF states, the preparation of fluorinated block alternating copolymers, as well as postsynthetic modifications.

Pesticidal compositions containing phosphoric esters and divalent sulphur compounds

Pesticidal composition comprising: a pesticidal, phosphoric ester the molecule of which has at least one alkyl group of 1 to 3 carbon atoms, 0.05 to 10% of an agent stabilizing the said ester against decomposition by protonisation, together with adjuvants characterized in that the stabilizing agent comprises at least one sulphur compound containing per molecule at least one divalent sulphur atom of which one valence is bonded to an atom chosen from sulphur, carbon, nitrogen, hydrogen, and metals capable of giving a salt, the other valence being bonded to an atom chosen from hydrogen, the carbon atom already noted, a second carbon atom, the nitrogen atom already noted, a second nitrogen atom, the metal atom already noted in the case of a metal of valence greater than one, a second atom of metal and oxygen when the first valence is not attached to an atom of hydrogen, the proportion of sulphur calculated with reference to the weight of the sulphur compound being between 5 and 99%. Process for stabilizing a phosphoric ester of which the molecule possesses at least one alkyl group containing 1 to 3 carbon atoms characterized in that there is added to the phosphoric ester or to a mixture which contains it, 0.05 to 10% calculated on the weight of the phosphoric acid ester of an agent capable of stabilizing the said phosphoric ester against protonisation and comprising at least one sulphur compound such as that defined thereupon.