813462-82-7 Usage
Imidazopyridazine class
It belongs to the class of imidazopyridazine compounds, which are known for their diverse biological activities and potential applications in medicinal chemistry.
Pyridazin-4-amine core
The compound contains a pyridazin-4-amine core, which is a key structural feature that may contribute to its potential pharmacological activities.
Potential applications in medicinal chemistry
Due to its structural features and potential pharmacological activities, this chemical may have applications in the development of new drugs and therapies.
Building block for synthesis
1H-Imidazo[4,5-d]pyridazin-4-amine, 7-methyl(9CI) can be used as a building block for the synthesis of various biologically active molecules, making it a valuable component in the creation of new pharmaceuticals.
Starting material for drug development
As a starting material, this compound can be used to develop new pharmaceuticals with potential therapeutic applications.
Need for further research
Further research and study are necessary to explore the potential uses and properties of 1H-Imidazo[4,5-d]pyridazin-4-amine, 7-methyl(9CI) in the field of pharmaceuticals and medicinal chemistry, in order to fully understand its potential and maximize its utility.
Check Digit Verification of cas no
The CAS Registry Mumber 813462-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,3,4,6 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 813462-82:
(8*8)+(7*1)+(6*3)+(5*4)+(4*6)+(3*2)+(2*8)+(1*2)=157
157 % 10 = 7
So 813462-82-7 is a valid CAS Registry Number.
813462-82-7Relevant articles and documents
Synthesis of 2-bromo-7-methyl-3,5-dihydro-imidazo[4,5-d]pyridazin-4-one and 3-alkyl-2-bromo-3,5-dihydro-imidazo[4,5-d]pyridazin-4-one and their selective elaboration
Eckhardt, Matthias,Hauel, Norbert,Langkopf, Elke,Himmelsbach, Frank
, p. 1931 - 1934 (2008/09/19)
Two synthetic routes to the versatile 3,5-dihydro-imidazo[4,5-d]pyridazin-4-ones 2 and 5 have been developed that allow the production of multigram quantities without the need of any chromatographic purification. Broad and selective elaboration of the heteroaromatic scaffolds has also been accomplished.
IMIDAZO-PYRIDAZINONE DERIVATIVES AND IMIDAZO-PYRIDONE DERIVATIVES, PRODUCTION THEREOF, AND USE THEREOF AS MEDICAMENTS
-
Page/Page column 43-44, (2008/06/13)
The invention relates to substituted imidazo-pyridinones and imidazo-pyridazinones of general formula (I), wherein Y and R1 to R4 are defined as indicated in claim 1, the tautomers, enantiomers, diastereomers, mixtures, and salts thereof that have valuable pharmacological properties, especially an inhibiting effect on the activity of the dipeptidyl peptidase IV (DPP-IV) enzyme.
