144660-63-9 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-methylpropyl)-α-phenyl-1H-imidazo[4,5-c]quinoline-2-methanol is used as a potential candidate in drug development due to its complex structure and pharmacological properties. Its unique molecular composition may allow for targeted interactions with specific biological receptors or enzymes, making it a promising compound for the creation of new medications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(2-methylpropyl)-α-phenyl-1H-imidazo[4,5-c]quinoline-2-methanol is used for further study and research. Its heterocyclic structure and functional groups may provide insights into the design and synthesis of new drugs with improved efficacy and selectivity.
Used in Chemical Research:
1-(2-methylpropyl)-α-phenyl-1H-imidazo[4,5-c]quinoline-2-methanol is also used as a subject of chemical research to explore its reactivity, stability, and potential applications in various chemical processes. 1-(2-methylpropyl)-α-phenyl-1H-imidazo[4,5-c]quinoline-2-methanol's solubility in organic solvents, due to the presence of the methanol group, may facilitate its use in synthesis and purification methods.
Used in Material Science:
The unique properties of 1-(2-methylpropyl)-α-phenyl-1H-imidazo[4,5-c]quinoline-2-methanol, such as its molecular structure and potential interactions with other molecules, may find applications in material science. It could be used in the development of new materials with specific properties, such as improved conductivity, strength, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 144660-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,6 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144660-63:
(8*1)+(7*4)+(6*4)+(5*6)+(4*6)+(3*0)+(2*6)+(1*3)=129
129 % 10 = 9
So 144660-63-9 is a valid CAS Registry Number.
144660-63-9Relevant academic research and scientific papers
1-substituted, 2-substituted 1H-imidazo[4,5-c]quinolin-4-amines
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Page column 22, (2010/02/04)
1-substituted, 2-substituted 1H-imidazo[4,5-c]-quinolin-4-amines are disclosed. These compounds function as antiviral agents, they induce biosynthesis of interferon, and they inhibit tumor formation in animal models. This invention also provides intermediates for preparing such compounds, pharmaceutical compositions containing such compounds, and pharmacological methods of using such compounds.
Process for preparing 1-substituted, 2-substituted 1H-imidazo[4, 5-c]quinoline-4-amines
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, (2008/06/13)
Methods of preparing 1-substituted, 2-substituted 1H-imidazo [4-5c]-quinolin-4-amines are disclosed. The compounds function as antiviral agents, they induce the biosynthesis of various cytokines including interferon, and they inhibit tumor formation in animal models.
1-substituted, 2-substituted 1H-imidazo[4,5-c]quinolin-4-amines
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, (2008/06/13)
1-substituted, 2-substituted 1H-imidazo[4,5-c]-quinolin-4-amines are disclosed. These compounds function as antiviral agents, they induce biosynthesis of interferon, and they inhibit tumor formation in animal models. This invention also provides intermediates for preparing such compounds, pharmaceutical compositions containing such compounds, and pharmacological methods of using such compounds.
Imidazo[4,5-c]quinolin-4-amines and processes for their preparation
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, (2008/06/13)
A process and intermediates for preparing 1-substituted-1H-imidazo[4,5-c]quinolin-4-amines. The process involves reacting a 1-substituted-1H-imidazo[4,5-c]quinoline-5N-oxide with an isocyanate and hydrolysing the product thereof. Also, a process for preparing the intermediates is disclosed.
