108310-79-8 Usage
Uses
Used in Pharmaceutical Synthesis:
Thiazolo[5,4-c]pyridin-2-amine is used as a key intermediate for the synthesis of various pharmaceuticals and agrochemicals, leveraging its versatile reactivity and potential pharmacological properties to contribute to the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
TPA is utilized as a subject of study in medicinal chemistry research, where it is explored for its potential antitumor and antiviral activities. Its unique structure and properties make it a promising candidate for the discovery of novel treatments and interventions in the medical field.
Used in Organic Synthesis:
Thiazolo[5,4-c]pyridin-2-amine is employed as a building block in organic synthesis, where its reactivity and structural features are harnessed to create a wide range of chemical compounds with diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 108310-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,1 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108310-79:
(8*1)+(7*0)+(6*8)+(5*3)+(4*1)+(3*0)+(2*7)+(1*9)=98
98 % 10 = 8
So 108310-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H5N3S/c7-6-9-4-1-2-8-3-5(4)10-6/h1-3H,(H2,7,9)
108310-79-8Relevant academic research and scientific papers
Iodine-catalyzed amination of benzothiazoles with KSeCN in water to access primary 2-aminobenzothiazoles
Zhu, Yu-Shen,Shi, Linlin,Fu, Lianrong,Chen, Xiran,Zhu, Xinju,Hao, Xin-Qi,Song, Mao-Ping
supporting information, p. 1497 - 1500 (2021/09/09)
A facile and sustainable approach for the amination of benzothiazoles with KSeCN using iodine as the catalyst in water has been disclosed under transition-metal free conditions. The reaction proceeded smoothly to afford various primary 2-amino benzothiazoles in up to 96% yield. A series of control experiments were performed, suggesting a ring-opening mechanism was involved via a radical process. This protocol provides efficient synthesis of primary 2-aminobenzothiazoles
