2,2′-Diphenylcarbonothioic dihydrazide, with the CAS number 622-03-7, is an organic compound characterized by its unique structure, which includes two phenyl groups attached to a carbonothioic acid moiety and two hydrazide functional groups. This compound typically appears as a solid and is known for its potential applications in various fields, including organic synthesis and as a reagent in chemical reactions. It exhibits properties such as moderate solubility in organic solvents and stability under standard laboratory conditions. The presence of hydrazide groups suggests that it may participate in condensation reactions, making it useful in the synthesis of more complex molecules. Additionally, its thioamide functionality can impart specific reactivity, particularly in nucleophilic substitution reactions. Safety data indicates that, like many hydrazine derivatives, it should be handled with care due to potential toxicity and reactivity. Overall, 2,2′-Diphenylcarbonothioic dihydrazide is a versatile compound with significant implications in synthetic chemistry.

2,2′-Diphenylcarbonothioic dihydrazide

622-03-7: 1,3-Dianilinothiourea, 1,5-Diphenylthiocarbohydrazide, 2,2′-Diphenylcarbonothioic dihydrazide, Carbohydrazide, 1,5-diphenyl-3-thio-, Carbonothioic dihydrazide, 2,2′-diphenyl-, Diphenyl Thiocarbazone, Diphenylthiocarbazide, N'',N'''-diphenylthiocarbonohydrazide, NSC 688

Diphenylthiocarbazide

Diphenylthiocarbazide is a reactive chemical that is soluble in water. It has been used as an injection solution and a model system for electron microscopic studies. The electron microscope was used to examine the reaction of Diphenylthiocarbazide with redox potentials, which are generated by the presence of a hydroxyl group. This chemical has also been used to study myeloid leukemia cells and tissue culture. The chloride ion can be extracted from hydrochloric acid when it reacts with Diphenylthiocarbazide. Nitrogen atoms may also be released during this process. The activation energies for these reactions are high, meaning they take a lot of energy to happen. Hydroxy groups on Diphenylthiocarbazide react with maternal blood cells, such as Hl-60 cells, to form free radicals and hydrogen peroxide that damage the cell membrane and lead to cell death.

CAS 622-03-7: 2,2′-Diphenylcarbonothioic dihydrazide

Diphenylthiocarbazide

Ref: IN-DA003PQ6

Diphenylthiocarbazide

Ref: 3D-FD166343

Diphenylthiocarbazide

Ref: 3B-D0917