81216-90-2 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
4-(3-BROMO-2-THIENYL)-1,3-THIAZOL-2-AMINE is used as a building block in the synthesis of new drugs, leveraging its unique molecular structure and properties. It has been studied for its potential as an anti-cancer and anti-inflammatory agent, making it a promising candidate for further research and development in the pharmaceutical industry.
Used in Cancer Treatment:
In the field of oncology, 4-(3-BROMO-2-THIENYL)-1,3-THIAZOL-2-AMINE is used as a potential anti-cancer agent, targeting various types of cancer. Its molecular structure allows it to interact with specific biological targets, potentially inhibiting cancer cell growth and proliferation.
Used in Inflammation Management:
4-(3-BROMO-2-THIENYL)-1,3-THIAZOL-2-AMINE is also used as a potential anti-inflammatory agent, which could be beneficial in treating various inflammatory conditions. Its ability to modulate inflammatory pathways may contribute to the development of new therapeutics for inflammatory diseases.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, 4-(3-BROMO-2-THIENYL)-1,3-THIAZOL-2-AMINE serves as a valuable chemical entity for the design and synthesis of novel therapeutic agents. Its unique structure and potential biological activities make it an attractive scaffold for the development of new drugs with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 81216-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,1 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81216-90:
(7*8)+(6*1)+(5*2)+(4*1)+(3*6)+(2*9)+(1*0)=112
112 % 10 = 2
So 81216-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrN2S2/c8-4-1-2-11-6(4)5-3-12-7(9)10-5/h1-3H,(H2,9,10)
81216-90-2Relevant academic research and scientific papers
BROMINATION OF 4-(2-THIENYL)THIAZOLES AND 2-(2-THIENYL)QUINOLINE
Smirnov, V. A.,Zimichev, A. V.,Lyzhova, G. A.,Lipkin, A. E.
, p. 28 - 31 (2007/10/02)
Depending on the substituent, the bromination of 4-(2-thienyl)thiazoles and 2-(2-thienyl)quinoline takes place in the 5 position of the thiophene or thiazole ring.When an amino group is present in the 2 position of the thiazole ring, bromination takes place in the 5 position of the thiazole ring.When excess brominating agent is present, a second bromine atom enters the 5 position of the free ring.
