66065-30-3

Usage

Uses

Used in Analytical Chemistry:
(2-chlorophenyl)carbamodithioic acid is used as a reagent for the determination of several metal ions, playing a crucial role in the analysis and detection of these elements.
Used in Industrial Processes:
In various industrial applications, (2-chlorophenyl)carbamodithioic acid serves as a chelating agent for metal ions, helping to manage and control the presence of these elements in different processes.
Used in Agriculture:
(2-chlorophenyl)carbamodithioic acid has demonstrated potential as both a fungicide and herbicide, effectively inhibiting the growth of certain microorganisms and plants, which can be beneficial in managing crop diseases and unwanted vegetation.
However, it is important to note that (2-chlorophenyl)carbamodithioic acid is considered to be moderately toxic. Therefore, it should be handled with care to avoid potential irritant and sensitizing effects on individuals who come into contact with it.

Upstream product

• 75-15-0 carbon disulfide 
• 95-51-2 o-chloroaniline 

Downstream Products

• 42135-75-1 4-(2'-chlorophenyl)-3-thiosemicarbazide 
• 23522-48-7 5-methyl-3-(2-chlorophenyl)-2-thioxothiazolidin-4-one 
• 1122513-16-9 C₉H₇ClNO₂S₂^(1-)*Na⁽¹⁺⁾ 
• 23522-47-6 2-mercapto-3-(o-chlorophenyl)-4-thiazolidone 

Relevant academic research and scientific papers

Novel rhodanines with anticancer activity: Design, synthesis and CoMSIA study

Three different series of some novel N-substituted rhodanines were designed for anticancer activity and prepared from the corresponding dithiocarbamates. The synthesized compounds were analyzed by IR, NMR and MASS to confirm their structures. All the titl

Catalytic dynamic spectrofluorimetry determination of trace antimony using new type arsenoxylphenylazo rhodanine

A precise, simple, new spectrofluorimetry method is proposed for determination of trace antimony which is based on the reaction between potassium periodate and the new type fluorescent reagent 3-o-chlorophenyl-5-(2′- arsenoxylphenylazo) rhodanine (2ClRAAP

Barriers to internal rotation around the C-N bond in 3-(o-aryl)-5-methyl- rhodanines using NMR spectroscopy and computational studies. Electron density topological analysis of the transition states

We have investigated the pairs of rotational isomers for six 3-(o-aryl)-5-methyl-rhodanines (Z = H, F, Cl, Br, OH, and CH3) using NMR spectroscopy and density functional theory (DFT) calculations. Electron density topological and NBO analysis h