77335-89-8 Usage
Explanation
The compound is composed of 13 carbon atoms, 14 hydrogen atoms, 2 nitrogen atoms, and 2 oxygen atoms.
Explanation
It belongs to a class of compounds derived from imidazole, a five-membered ring containing two nitrogen atoms.
Explanation
The phenyl ring (a six-membered carbon ring with alternating single and double bonds) has a methoxy group (-OCH3) attached to it, which is a methyl group with an oxygen atom attached.
Explanation
The compound features a 1H-imidazole ring, which is a five-membered ring with one nitrogen atom and two hydrogen atoms. A methyl group (-CH3) is attached to this ring.
Explanation
The compound also contains an ethanone group (also known as acetone group), which is a carbonyl group (C=O) attached to an ethyl group (CH3-CH2-).
Explanation
The compound is utilized in the pharmaceutical industry and research settings, with its specific properties and uses varying depending on the context in which it is employed.
Explanation
The solubility of 1-[2-(4-methoxyphenyl)-4-methyl-1H-imidazol-5-yl]Ethanone can differ based on the solvent used, which can impact its applications and handling.
Explanation
The stability of the compound can be influenced by factors such as temperature, light, and humidity, which may affect its shelf life and storage requirements.
Explanation
Due to its functional groups, 1-[2-(4-methoxyphenyl)-4-methyl-1H-imidazol-5-yl]Ethanone can undergo various chemical reactions with different reagents, which can be exploited in synthesis and pharmaceutical applications.
Explanation
The purity of the compound is crucial for its effectiveness and safety in pharmaceutical and research settings, as impurities can lead to unwanted side effects or inaccurate results.
Classification
Imidazole derivative
Phenyl ring
Contains a methoxy group
1H-imidazole ring
With a methyl group attached
Ethanone group
Present in the structure
Pharmaceutical and research applications
Used in various contexts
Solubility
May vary depending on the solvent
Stability
May be sensitive to certain conditions
Reactivity
Can react with various reagents
Purity
Important for pharmaceutical and research applications
Check Digit Verification of cas no
The CAS Registry Mumber 77335-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77335-89:
(7*7)+(6*7)+(5*3)+(4*3)+(3*5)+(2*8)+(1*9)=158
158 % 10 = 8
So 77335-89-8 is a valid CAS Registry Number.
77335-89-8Relevant academic research and scientific papers
β1-Selective Adrenoceptor Antagonists: Examples of the 2-phenyl>imidazole Class. 2
Baldwin, John J.,Christy, Marcia E.,Denny, George H.,Habecker, Charles N.,Freedman, Mark B.,et al.
, p. 1065 - 1080 (2007/10/02)
An attempt to develop a highly cardioselective β-adrenoceptor antagonist devoid of intrinsic sympathomimetic activity (ISA) focused on exploring structure-activity relationships around (S)--amino>-2-hydroxypropoxy>phen
Syntheses of 2-Arylimidazole Derivatives through Annelations Employing Benzylamines
Veronese, A.C.,Cavicchioni, G.,Servadio, G.,Vecchiati, G.
, p. 1723 - 1725 (2007/10/02)
Annelations of benzylamines with hydroximino derivatives of pentane-2,4-dione or of alkyl acetoacetates, acetoacetamides, and acetoacetanilides, afford imidazole derivatives and provide easy incorporation of the benzylic carbon and nitrogen in the heterocycle.The limits of the reaction have been explored.
