2740-95-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1,3-dimethyl-1-phenylthiourea is utilized as a catalyst in the synthesis of various pharmaceuticals and agrochemicals. Its ability to facilitate organic reactions contributes to the production of a wide range of therapeutic agents and agricultural products.
Used in Rubber and Plastics Production:
1,3-dimethyl-1-phenylthiourea is employed in the manufacturing process of rubber and plastics, where it serves as a catalyst to enhance the efficiency and quality of the final products.
Used in Antioxidant Applications:
1,3-dimethyl-1-phenylthiourea has been studied for its potential as an antioxidant, demonstrating promising results in scavenging free radicals and inhibiting lipid peroxidation. This property makes it a candidate for use in applications where protection against oxidative stress is required.
However, it is crucial to handle 1,3-dimethyl-1-phenylthiourea with care, as it is toxic if ingested and may cause skin and eye irritation upon contact. Proper safety measures should be taken to minimize the risk of adverse effects during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2740-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2740-95:
(6*2)+(5*7)+(4*4)+(3*0)+(2*9)+(1*5)=86
86 % 10 = 6
So 2740-95-6 is a valid CAS Registry Number.
2740-95-6Relevant academic research and scientific papers
Activation of Dithiocarbamate by 2-Halothiazolium Salts
Sugimoto, Hirohiko,Makino, Itsuo,Hirai, Kentaro
, p. 2263 - 2267 (2007/10/02)
Activation of dithiocarbamate salts with 2-halo-3-alkyl-4-phenylthiazolium salt and subsequent one-pot nucleophilic reaction with N, S, and O nucleophiles provided substituted thioureas, dithiocarbamates, and thiocarbamates or amides, respectively, under very mild conditions.A useful thiocarbonyl-transfer reaction is also described that consists of activation of imidazolodithiocarbamate and a subsequent one-pot nucleophilic reaction. (Thiocarbonyl)diimidazole is generated in situ.
