2829-57-4 Usage
Uses
Used in Pharmaceutical Industry:
[1,2,5]Thiadiazolo[3,4-d]pyrimidin-7-amine is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure and potential bioactivity make it a promising candidate for the synthesis of therapeutic agents that could target a range of medical conditions.
Used in Chemical Synthesis:
In the field of chemical synthesis, [1,2,5]Thiadiazolo[3,4-d]pyrimidin-7-amine serves as a building block for the creation of more complex chemical compounds. Its ability to be integrated into larger molecular structures allows for the development of novel compounds with specific properties and applications.
Used in Materials Science:
[1,2,5]Thiadiazolo[3,4-d]pyrimidin-7-amine may also find applications in materials science, where its unique structure could contribute to the development of new materials with specialized properties. These materials could be used in various industries, such as electronics, energy, or advanced manufacturing.
Used in Technological Development:
[1,2,5]Thiadiazolo[3,4-d]pyrimidin-7-amine's potential applications extend to the development of new technologies, where its unique properties could be harnessed to create innovative solutions in areas such as sensors, catalysts, or other high-tech applications.
Overall, [1,2,5]Thiadiazolo[3,4-d]pyrimidin-7-amine is a versatile and intriguing compound with a broad spectrum of potential uses across different industries. Its continued study and development could lead to significant advancements in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 2829-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2829-57:
(6*2)+(5*8)+(4*2)+(3*9)+(2*5)+(1*7)=104
104 % 10 = 4
So 2829-57-4 is a valid CAS Registry Number.
2829-57-4Relevant academic research and scientific papers
Process for preparation of 9-(dihalobenzyl) adenines
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, (2008/06/13)
9-(Dihalobenzyl)adenines are prepared uncontaminated with other positional isomers in a series of mild transformations starting from 4,5,6-triaminopyrimidine and proceeding via 7-(N-formyl-N-dihalobenzyl)amino[1,2,5]thiadiazolo[3,4-d]pyrimidine. The resulting compounds have anticoccidial activity and are useful in controlling cecal and/or intestinal coccidiosis when administered in minor quantities to animals, in particular to poultry usually in admixture with animal sustenance.
