202278-29-3 Usage
Uses
Used in Pharmaceutical Development:
1,5-Dihydro-1,7-dimethyl-4H-imidazo[4,5-d]pyridazin-4-one is used as a chemical building block for the development of novel pharmaceutical drugs. Its unique structure allows for the design of new molecules with potential therapeutic effects, contributing to advancements in medicine.
Used in Biochemical Research:
In the field of biochemical research, 1,5-Dihydro-1,7-dimethyl-4H-imidazo[4,5-d]pyridazin-4-one serves as a research tool. Its distinctive structural features make it suitable for studying various biological processes and interactions, aiding in the discovery of new mechanisms and potential drug targets.
While the specific applications and properties of 1,5-Dihydro-1,7-dimethyl-4H-imidazo[4,5-d]pyridazin-4-one in different scientific and technological domains are still under investigation, its potential in these areas highlights its importance in ongoing research and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 202278-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,2,7 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 202278-29:
(8*2)+(7*0)+(6*2)+(5*2)+(4*7)+(3*8)+(2*2)+(1*9)=103
103 % 10 = 3
So 202278-29-3 is a valid CAS Registry Number.
202278-29-3Relevant academic research and scientific papers
AZOLE-FUSED PYRIDAZIN-3(2H)-ONE DERIVATIVES
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Paragraph 0348; 0349, (2021/04/01)
Disclosed are compounds of Formula (1) and pharmaceutically acceptable salts thereof, wherein α, β, n, R4, R5, R6, R8, R9, R10, R11, X1, X2, X3 and X7 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula (1), to pharmaceutical compositions comprising them, and to their use for treating diseases, disorders, and conditions associated with GPR139.
New transformations of heterocycles illustrated by the example of imidazo[4,5-c]pyridine derivatives
Yutilov,Svertilova
, p. 583 - 584 (2007/10/03)
1-Alkyl-7-nitroimidazo[4,5-c]pyridin-4-ones with excess hydrazine hydrate furnish 1-alkyl-7-methylimidazo[4,5-d]pyridazin-4-ones in high yields. The reaction presumably proceeds as forcing out the 6-methine group from the pyridine ring of the original mol
