89185-48-8 Usage
Uses
Used in Medicinal Chemistry:
2-Phenyl-imidazo[1,2-a]pyrimidin-3-ylamine is used as a potential drug candidate for the treatment of various diseases, particularly in the areas of cancer and inflammation. Its biological activity and potential as a kinase inhibitor make it a valuable candidate for the development of new therapeutic drugs.
Used in Cancer Research:
In the field of cancer research, 2-Phenyl-imidazo[1,2-a]pyrimidin-3-ylamine is used as a potential kinase inhibitor, which could play a crucial role in the development of new cancer treatments. Its ability to target specific cellular pathways and inhibit the growth of cancer cells makes it a promising candidate for further research and drug development.
Used in Inflammation Research:
2-Phenyl-imidazo[1,2-a]pyrimidin-3-ylamine is also used in the study of inflammation, where it has shown potential as a therapeutic agent for the treatment of inflammatory diseases. Its ability to modulate inflammatory pathways and reduce inflammation-related symptoms makes it a valuable candidate for further research and potential drug development in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 89185-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,8 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89185-48:
(7*8)+(6*9)+(5*1)+(4*8)+(3*5)+(2*4)+(1*8)=178
178 % 10 = 8
So 89185-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N4/c13-11-10(9-5-2-1-3-6-9)15-12-14-7-4-8-16(11)12/h1-8H,13H2
89185-48-8Relevant academic research and scientific papers
Cyclisation Reactions of some 3-Nitrosoimidazo-pyridines and -pyrimidines. Ring-opening/Ring-closure Reactions with Triethyl Phosphite: Reassignment by X-Ray Crystal Structure and Nuclear Magnetic Resonance
Teulade, Jean C.,Escale, Roger,Viols, Henry,Chapat, Jean P.,Grassy, Gerard,et al.
, p. 2663 - 2667 (2007/10/02)
Deoxygenation of 3-nitroso-2-phenylimidazo-pyridines and -pyrimidines with triethyl phosphite does not lead to the products described in the literature as pyrido- and pyrimido-imidazoindoles (3) and (4), but to the open-chain derivatives, N-(2-pyri
