2741-14-2 Usage
Description
3-Benzyl-1,1-dimethylthiourea is a chemical compound with the molecular formula C11H16N2S. It is a thiourea derivative featuring a benzyl group and two methyl groups attached to the nitrogen atom. 3-benzyl-1,1-dimethylthiourea is recognized for its antioxidant and anti-inflammatory properties, which contribute to its potential use in pharmaceutical research and development.
Uses
Used in Pharmaceutical Research:
3-Benzyl-1,1-dimethylthiourea is utilized as a reagent in organic synthesis and pharmaceutical research. Its antioxidant and anti-inflammatory properties make it a promising candidate for the development of new drugs to treat various medical conditions.
Used in Neurodegenerative Disease Treatment:
In the medical field, 3-benzyl-1,1-dimethylthiourea is studied for its potential applications in the treatment of neurodegenerative diseases. Its capacity to exhibit neuroprotective effects positions it as a candidate for further research and development in this area.
Used in Cancer Treatment:
Additionally, 3-benzyl-1,1-dimethylthiourea has been investigated for its potential role in cancer treatment. 3-benzyl-1,1-dimethylthiourea's properties are being explored to understand its impact on cancer cells and its possible use in therapeutic strategies against cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 2741-14-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 2741-14:
(6*2)+(5*7)+(4*4)+(3*1)+(2*1)+(1*4)=72
72 % 10 = 2
So 2741-14-2 is a valid CAS Registry Number.
2741-14-2Relevant articles and documents
Insertion of arynes into thioureas: A new amidine synthesis
Biswas, Kallolmay,Greaney, Michael F.
supporting information; experimental part, p. 4946 - 4949 (2011/11/06)
Arynes, generated from trimethylsilyl phenyltriflate precursors, have been found to react with thioureas via a formal π-insertion into the C=S bond. The reaction contrasts with that of ureas, which proceeds via benzyne σ-insertion into the C-N bond, and r
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
