79938-46-8 Usage
Bicyclic compound
The benzimidazole core structure consists of two fused rings, which contribute to its stability and potential applications in various fields.
Derivative of benzimidazole
1H-benzimidazole, 1-acetyl-5-methoxyis a modified version of the parent compound benzimidazole, with additional functional groups that may alter its properties and potential uses.
Acetyl group (CH3CO-)
A acetyl group is attached to the benzimidazole core structure, which is an acetic acid derivative. This group may contribute to the compound's reactivity and potential applications in medicinal chemistry.
Methoxy group (OCH3-)
A methoxy group is also attached to the benzimidazole core structure, which is a methyl ether derivative. This group may influence the compound's solubility, stability, and biological activity.
Biological activities
Due to its structural features, 1H-benzimidazole, 1-acetyl-5-methoxyis likely to exhibit various biological activities, such as enzyme inhibition, receptor binding, or other interactions with biological systems.
Potential applications
The compound may have potential applications in medicinal and agricultural chemistry, as its structural features and biological activities could be harnessed for therapeutic or pesticidal purposes.
Further research needed
To fully understand the properties and potential uses of 1H-benzimidazole, 1-acetyl-5-methoxy-, further studies and research are required, including in vitro and in vivo testing, as well as investigation of its mechanism of action and potential side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 79938-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,3 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79938-46:
(7*7)+(6*9)+(5*9)+(4*3)+(3*8)+(2*4)+(1*6)=198
198 % 10 = 8
So 79938-46-8 is a valid CAS Registry Number.
79938-46-8Relevant articles and documents
Synthesis of N-Acetylbenzimidazole Derivatives
Tanaka, Kenjiro,Shimazaki, Michiko,Murakami, Yasuoki
, p. 2714 - 2722 (2007/10/02)
For the structure determination of thiazolobenzimidazol-3(2H)-one derivatives (2 or 3) they were converted to the corresponding 1-acetylbenzimidazoles (4) by desulfurization.The latter compounds (4) were alternatively prepared by the cyclization of 2-aminoacetanilide derivatives (5) with CS2 in dimethylformamide (DMF), followed by desulfurization with Raney Ni.However, the reactions of 5 with ethyl orthoformate/H2SO4 in DMF gave a mixture of 4 and its acetyl-rearranged product (7).Keywords-acetyl group; rearrangement; thiazolobenzimidazol-3(2H)-one; N-acetylbenzimidazoles; ethyl orthoformate; carbon disulfide; desulfurization
