20821-66-3

Usage

Uses

Used in Rubber and Plastics Industry:
DIMETHYLDITHIOCARBAMIC ACID ALLYL ESTER is used as a vulcanization accelerator for the production of rubber and plastics. It facilitates the cross-linking of polymer chains, which is crucial for improving the strength and elasticity of the final product.
Used in Industrial Biocides:
DIMETHYLDITHIOCARBAMIC ACID ALLYL ESTER is used as a biocide to inhibit the growth of microorganisms in certain industrial processes. This application helps maintain the integrity and quality of products by preventing microbial contamination.

InChI:InChI=1/C6H11NS2/c1-4-5-9-6(8)7(2)3/h4H,1,5H2,2-3H3

Upstream product

• 107-05-1 3-chloroprop-1-ene 
• 128-04-1 sodium dimethyldithiocarbamate 
• 75-15-0 carbon disulfide 
• 124-40-3 dimethyl amine 

Downstream Products

• 56281-58-4 Dimethyl-dithiocarbamic acid (E)-1-benzyl-but-2-enyl ester 
• 53282-00-1 trans-(4-Phenyl-buten-⁽²⁾-yl)dithiocarbamat 
• 56281-53-9 Dimethyl-dithiocarbamic acid 1-benzyl-allyl ester 
• 84766-41-6 Dimethyl-dithiocarbamic acid 1-[1-(4-cyano-phenyl)-1-hydroxy-ethyl]-allyl ester 
• 84766-42-7 Dimethyl-dithiocarbamic acid (Z)-4-(4-cyano-phenyl)-4-hydroxy-pent-1-enyl ester 
• 84766-42-7 Dimethyl-dithiocarbamic acid (E)-4-(4-cyano-phenyl)-4-hydroxy-pent-1-enyl ester 
• 84766-37-0 Dimethyl-dithiocarbamic acid 1-[1-(4-fluoro-phenyl)-1-hydroxy-ethyl]-allyl ester 
• 84766-38-1 Dimethyl-dithiocarbamic acid (Z)-4-(4-fluoro-phenyl)-4-hydroxy-pent-1-enyl ester 
• 84766-38-1 Dimethyl-dithiocarbamic acid (E)-4-(4-fluoro-phenyl)-4-hydroxy-pent-1-enyl ester 
• 84766-39-2 Dimethyl-dithiocarbamic acid 1-[1-(4-chloro-phenyl)-1-hydroxy-ethyl]-allyl ester 
• 84766-40-5 Dimethyl-dithiocarbamic acid (Z)-4-(4-chloro-phenyl)-4-hydroxy-pent-1-enyl ester 
• 84766-40-5 Dimethyl-dithiocarbamic acid (E)-4-(4-chloro-phenyl)-4-hydroxy-pent-1-enyl ester 
• 84766-45-0 Dimethyl-dithiocarbamic acid 1-[hydroxy-(4-methoxy-phenyl)-methyl]-allyl ester 
• 84766-46-1 Dimethyl-dithiocarbamic acid (Z)-4-hydroxy-4-(4-methoxy-phenyl)-but-1-enyl ester 

Relevant academic research and scientific papers

Regiospecific iodocyclization of S-allyl dithiocarbamates: synthesis of 2-imino-1,3-dithiolane and 2-iminium-1,3-dithiolane derivatives

4-Alkyl-2-imino-1,3-dithiolanes and 4-alkyl-2-iminium-1,3-dithiolanes were prepared in excellent yields with complete regiospecificity under mild conditions by the iodocyclization of S-allyl dithiocarbamates. Dehydrohalogenation of the 4-alkyl-2-imino-1,3

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.