2741-12-0 Usage
Description
1,1-dimethyl-3-(2-methylphenyl)thiourea is a chemical compound with the molecular formula C11H16N2S. It is a thiourea derivative characterized by a dimethyl-substituted terminal nitrogen and a 2-methylphenyl group. 1,1-dimethyl-3-(2-methylphenyl)thiourea is recognized for its potential applications across various industries, including as a catalyst and intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. Additionally, it exhibits biological activities such as anti-inflammatory and antioxidant properties, which further broaden its scope of use. However, due to potential health risks, careful handling, management, and disposal are essential.
Uses
Used in Catalyst Industry:
1,1-dimethyl-3-(2-methylphenyl)thiourea serves as a catalyst, facilitating various chemical reactions in the synthesis of different organic compounds. Its unique structure allows it to effectively lower activation energy and increase reaction rates, making it a valuable component in the production process.
Used in Pharmaceutical Industry:
As an intermediate in pharmaceutical production, 1,1-dimethyl-3-(2-methylphenyl)thiourea plays a crucial role in the synthesis of various medicinal compounds. Its involvement in the creation of new drugs highlights its importance in the development of novel treatments and therapies.
Used in Dye Industry:
1,1-dimethyl-3-(2-methylphenyl)thiourea is utilized as an intermediate in the production of dyes, contributing to the development of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.
Used in Organic Compounds Synthesis:
1,1-dimethyl-3-(2-methylphenyl)thiourea is also employed in the synthesis of other organic compounds, showcasing its versatility and applicability in the broader field of organic chemistry.
Used in Biological Research:
Due to its anti-inflammatory and antioxidant properties, 1,1-dimethyl-3-(2-methylphenyl)thiourea is used in biological research to explore its potential as a therapeutic agent. Studies on its biological activities can lead to the discovery of new treatments for various conditions and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 2741-12-0 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 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2741-12:
(6*2)+(5*7)+(4*4)+(3*1)+(2*1)+(1*2)=70
70 % 10 = 0
So 2741-12-0 is a valid CAS Registry Number.
2741-12-0Relevant articles and documents
Use of tetramethylthiuram disulfide in synthesis of nitrogen-containing heterocyclic compounds
Demchenko,Yanchenko,Kisly,Lozinskii
, p. 668 - 672 (2007/10/03)
We have developed a method for synthesis of aryl isothiocyanates by means of thiocarbamoylation of aromatic amines by tetramethylthiuram disulfide followed by degradation of the intermediate N(1)-aryl-N,N- dimethylthiourea by concentrated HCl. We have shown that thiocarbamoylation of 4-amino-5-ethyl-4H-1,2,4-triazole-3-thiol occurs at the 2 position of the triazole ring, while thiocarbamoylation of 4-amino-3-methyl-6-phenyl-4,5- dihydro-1,2,4-triazin-5-one leads to the dihetaryl-substituted thiourea. We consider the possibility of using N(1)-aryl-N,N-dimethylthioureas as analogs of isothiocyanates in reactions with N-nucleophiles. 2005 Springer Science+Business Media, Inc.
A convenient route to substituted thiocarbamides
Ramadas,Srinivasan
, p. 3381 - 3387 (2007/10/03)
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