51808-84-5 Usage
Uses
Used in Organic Chemistry:
2-(bromomethyl)-2,3,6,7,8,9-hexahydro-5H-[1]benzothieno[2,3-d][1,3]thiazolo[3,2-a]pyrimidin-5-one is used as a building block for the synthesis of other organic compounds, leveraging its reactive bromomethyl group and complex ring systems to form novel molecular structures.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(bromomethyl)-2,3,6,7,8,9-hexahydro-5H-[1]benzothieno[2,3-d][1,3]thiazolo[3,2-a]pyrimidin-5-one is used as a starting material for the development of new drugs. Its structural features may contribute to the creation of potential therapeutic agents, particularly in the areas of medicinal chemistry where its reactivity and interaction with biological targets are of interest.
Used in Industrial Applications:
2-(bromomethyl)-2,3,6,7,8,9-hexahydro-5H-[1]benzothieno[2,3-d][1,3]thiazolo[3,2-a]pyrimidin-5-one may also find use in industrial applications where its chemical properties are harnessed for the production of specialty materials or intermediates in chemical processes. Its potential reactivity and structural attributes could be exploited in the synthesis of advanced materials or as part of larger chemical systems. Further research and testing are necessary to fully explore and understand its capabilities and potential uses in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 51808-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,0 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51808-84:
(7*5)+(6*1)+(5*8)+(4*0)+(3*8)+(2*8)+(1*4)=125
125 % 10 = 5
So 51808-84-5 is a valid CAS Registry Number.
51808-84-5Relevant academic research and scientific papers
Sauter,Deinhammer,Danksagmueller
, p. 863 - 868 (1974)
The title substances and their [1]benzothieno analogues were synthesized by reaction of 3-allyl-2-mercapto-([1]benzo)thieno-[2.3-d]pyrimidine-4(3 H)-ones with Br2 to 2-bromomethyl-2.3-dihydro-thiazolo[3.2-a]([1]benzo-)thieno[2.3-d]pyrimidine-5-ones, which on treatment with morpholine did not give the corresponding morpholine derivatives but elimination to the exocyclic double bond. These 2-methylene-2.3-dihydro-products were isomerized by H2SO4 to the corresponding 2-methyl compounds.
Khripak, S. M.,Yakubets, V. I.,Dobosh, A. A.,Migalina, Yu. V.
, p. 915 - 918 (1987)
The reaction of mercury salts with thienopyrimidine derivatives was studied.It was shown that even in nucleophilic solvents the solvatomercuration of thienopyrimidines is accompanied by intramolecular ring closure involving the sulfur atom of the thioureide group.
