6327-27-1

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

It is classified as an organic compound because it contains carbon and hydrogen atoms.

Explanation

The compound has a complex structure made up of different functional groups, which contribute to its chemical properties and reactivity.

Explanation

It is derived from thiourea, which is a simple organic compound containing a disulfide group.

Explanation

Due to its unique structure and properties, the compound is utilized in a wide range of chemical reactions and synthesis processes.

Explanation

Its versatility in chemical reactions makes it a valuable reagent for synthesizing various products, including pharmaceuticals, dyes, and other organic compounds.

Explanation

The compound's ability to act as both a nucleophile (electron pair donor) and an electrophile (electron pair acceptor) makes it useful in a wide range of chemical reactions.

Explanation

As with many chemicals, it is essential to handle 1,3-bis[[(Z)-(6-oxo-1-cyclohexa-2,4-dienylidene)methyl]amino]thiourea carefully to minimize the risk of exposure and potential health hazards. Proper safety measures should be taken when working with 1,3-bis[[(Z)-(6-oxo-1-cyclohexa-2,4-dienylidene)methyl]amino]thiourea.

Type of compound

Organic compound

Structure

Complex structure consisting of cyclohexadiene, amino, and thiourea functional groups

Derivative of

Thiourea

Applications

Used in various chemical reactions and organic synthesis processes

Common use

As a reagent in the production of pharmaceuticals, dyes, and organic compounds

Chemical properties

Exhibits strong nucleophilic and electrophilic properties

Safety precautions

Handle with caution due to potential health risks

Upstream product

• 38650-90-7 thiocarbohydrazide hydrochloride 
• 90-02-8 salicylaldehyde 
• 2231-57-4 Thiocarbohydrazide 

Relevant academic research and scientific papers

Hartree-Fock, molecular docking, spectral, kinetic and antitumor considerations for cobalt, nickel, palladium and platinum (II)-bis carbothiohydrazide complexes

New metal ion complexes were synthesized using Schiff base derivative and characterized using spectral and theoretical analysis. IR and 1H NMR spectra, suggest bi-dentate to tetra-dentate mode of bonding each towards two metal ions. Square-planar and octa

SEPARATION AND DETERMINATION OF PARTS-PER-BILLION CONCENTRATIONS OF GALLIUM IN BIOLOGICAL MATERIALS.

Gallium is separated from an aqueous digest of a biological matrix, by the selective extraction of the ion pair GaCl//4** minus multiplied by (times) R//4N** plus , into a hexane-methyl isobutyl ketone mixture (R//4N** plus represents the methyltricapryla

1,3-Bis(salicylidineamino)thiourea dihydrate as an analytical reagent for the direct spectrophotometric determination of Co(II) in natural samples

A simple, rapid, selective and sensitive spectrophotometric method for the determination of microamounts of Co(II), alone or in presence of associated metals has been developed.Co(II) forms a 1:2 complex with 1,3-bis(salicylidineamino)thiourea dihydrate w

Synthesis and Characterization of Bis-thiocarbonohydrazones

Several bis-thiocarbonohydrazones have been synthesized using improved methods.The compounds prepared have been characterized by elemental analyses, melting points, and IR and PMR spectra.

MAGNETIC AND SPECTRAL PROPERTIES OF NICKEL(II) COMPLEXES WITH THIOCARBOHYDRAZONES

Nickel(II) complexes of thiocarbohydrazones were prepared by reacting nickel(II) chloride with the appropriate thiocarbohydrazones in an alcoholic medium.The complexes are brownish in colour and analyze for 1:1 stoichiometry of the type NiL.The molecular weight determination in nitrobenzene indicates that the complexes are monomeric in nature.These are diamagnetic, and optical spectra support this conclusion.The infrared spectra of the complexes compared with those of the ligands suggest that hydroxy groups of the ligands are involved in bond formation with the Ni(II) moiety via deprotonation.The -C=N groups form coordinate bonds through N atom of the azomethine group.The S atom of the ligand does not take part in coordinate bond formation.Assignments have been made in the low frequency region (600-200 cm-1).The various bands found in this region are assigned to ν(Ni-N) and γ(NiO) modes.All these observations point to a square planar configuration for these complexes and focus upon non-involvement of the -S- group in the bond.Thus ligands in these complexes show a tetradentate behaviour by keeping the S group away from coordination.