598-64-1 Usage
Description
DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT, with the chemical formula (CH3)2NCS2–CH3, is a versatile chemical compound that serves as a fungicide and bactericide in various applications. It is effective in inhibiting the growth and reproduction of microorganisms, making it a valuable asset in agricultural and industrial settings.
Uses
Used in Agricultural Applications:
DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT is used as a fungicide and bactericide for controlling fungal and bacterial infections in crops and other plants. It helps protect plants from diseases and ensures a healthy growth, contributing to increased crop yields.
Used in Industrial Applications:
DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT is used as a biocide in industrial water treatment, where it helps control the growth of microorganisms that can cause fouling, corrosion, and other issues in water systems. This ensures the efficient operation of industrial processes that rely on water.
Used in Wood Preservation:
DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT is used as a preservative for wood and other materials, protecting them from fungal and bacterial attacks. This extends the lifespan of wooden structures and products, reducing the need for frequent replacements and maintenance.
It is important to handle DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT with care, as it can be toxic if ingested or absorbed through the skin, and can be harmful to aquatic organisms if it enters waterways. Proper safety measures should be taken during its use to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 598-64-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 598-64:
(5*5)+(4*9)+(3*8)+(2*6)+(1*4)=101
101 % 10 = 1
So 598-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NS2.C2H7N/c1-4(2)3(5)6;1-3-2/h1-2H3,(H,5,6);3H,1-2H3
598-64-1Relevant articles and documents
Cu-mediated one-pot three-component synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives
Dong, Wei,Ge, Zemei,Wang, Xin,Li, Ridong,Li, Runtao
, (2020/07/03)
A novel and efficient copper-catalyzed one-pot procedure for the synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives from 2-halobenzenesulfonamides, amines and CS2 is described. The reaction proceeds through Ullmann-type S-arylation, intramolecular addition of NH2 with C[dbnd]S and dehydrosulfide, which provides a new and useful strategy for construction of cyclic aromatic sulfonamides.
Utilization of carbon disulfide as a powerful building block for the synthesis of 2-aminobenzoxazoles
Guntreddi, Tirumaleswararao,Allam, Bharat Kumar,Singh, Krishna Nand
, p. 9875 - 9880 (2013/09/02)
This protocol describes a novel, mild and convenient route to afford 2-aminobenzoxazoles in high yields, and represents a significant advance towards an environmentally friendly strategy. Aliphatic amines are made to react with carbon disulfide to provide intermediate dithiocarbamates (DTC), which in the presence of 2-aminophenol, subsequently undergo successive intermolecular nucleophilic attack and desulfurization to produce 2-aminobenzoxazoles within 3 h.
Thiocarbamoylation of amine-containing compounds 4. Reactions of tetramethylthiuram disulfide with aliphatic amines
Van Boi, Luu
, p. 2294 - 2298 (2007/10/03)
Thiocarbamoylation of primary and secondary aliphatic amines with tetramethylthiuram disulfide in various solvents at different temperatures was studied. At 110 °C, the reactions with primary amines afforded mixed N,N-dimethyl-N′-alkyl(cycloalkyl)thiourea