136228-41-6 Usage
Uses
Used in Pharmaceutical Synthesis:
2H-1,2-Thiazine,3,6-dihydro-4,5-dimethyl-2-(1-methylethyl)-(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to serve as a building block for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Production:
In the agrochemical industry, 2H-1,2-Thiazine,3,6-dihydro-4,5-dimethyl-2-(1-methylethyl)-(9CI) is utilized as a precursor in the production of various agrochemicals. Its incorporation into these products can contribute to the development of more effective and targeted pest control solutions.
Used in Disease Treatment Research:
2H-1,2-Thiazine,3,6-dihydro-4,5-dimethyl-2-(1-methylethyl)-(9CI) is being studied for its potential use in the treatment of various diseases, such as cancer and neurodegenerative disorders. Its unique chemical properties may offer new avenues for therapeutic intervention and drug development in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 136228-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,2 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136228-41:
(8*1)+(7*3)+(6*6)+(5*2)+(4*2)+(3*8)+(2*4)+(1*1)=116
116 % 10 = 6
So 136228-41-6 is a valid CAS Registry Number.
136228-41-6Relevant academic research and scientific papers
N-TRIMETHYLSILYL-N-CHLOROTHIOALKYLAMINES IN SYNTHESES OF ALKYLTHIONITROSO COMPOUNDS
Markovskii,L. N.,Solov'ev, A. V.,Kaminskaya, E. I.,Borodin, A. V.,Shermolovich, Yu. G.
, p. 1799 - 1801 (2007/10/02)
The thermal stability of N-trimethylsilyl-N-chlorothioalkylamines, which are formed in the reaction of N-trimethylsilylamines with sulfur dichloride in the presence of triethylamine, is determined by the size of the alkyl substituent and increases with increase in the size.The thermolysis of N-trimethylsilyl-N-chlorothio-tert-butyl- and N-trimethylsilyl-N-chlorothioisopropylamines leads to the formation of thionitrosoalkanes.The latter were identified in the form of the products from cycloaddition with 2,3-dimethyl-1,3-butadiene, i.e., 2-alkyl-4,5-dimethyl-3,6-dihydro-1,2-thiazines.
