97968-80-4 Usage
Description
2-Cyclobutylbenzimidazole is a chemical compound with the molecular formula C13H14N2. It is a benzimidazole derivative that contains a cyclobutyl group in its structure. This chemical has been studied for its potential pharmacological activities, including its use as a building block in the synthesis of pharmaceutical compounds. It has been found to exhibit antiviral, anti-inflammatory, and anticancer properties. 2-Cyclobutylbenzimidazole has also been investigated for its potential as a photochromic material, showing reversible photoisomerization behavior. Overall, this chemical compound has shown promise in various research fields and may have potential applications in the pharmaceutical and materials industries.
Uses
Used in Pharmaceutical Industry:
2-Cyclobutylbenzimidazole is used as a building block for the synthesis of pharmaceutical compounds due to its antiviral, anti-inflammatory, and anticancer properties.
Used in Materials Industry:
2-Cyclobutylbenzimidazole is used as a photochromic material for its reversible photoisomerization behavior, which may have potential applications in various materials research fields.
Check Digit Verification of cas no
The CAS Registry Mumber 97968-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,6 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97968-80:
(7*9)+(6*7)+(5*9)+(4*6)+(3*8)+(2*8)+(1*0)=214
214 % 10 = 4
So 97968-80-4 is a valid CAS Registry Number.
97968-80-4Relevant articles and documents
Metal-Free-Visible Light C-H Alkylation of Heteroaromatics via Hypervalent Iodine-Promoted Decarboxylation
Genovino, Julien,Lian, Yajing,Zhang, Yuan,Hope, Taylor O.,Juneau, Antoine,Gagné, Yohann,Ingle, Gajendra,Frenette, Mathieu
supporting information, p. 3229 - 3232 (2018/06/11)
A metal-free photoredox C-H alkylation of heteroaromatics from readily available carboxylic acids using an organic photocatalyst and hypervalent iodine reagents under blue LED light is reported. The developed methodology tolerates a broad range of functional groups and can be applied to the late-stage functionalization of drugs and drug-like molecules. The reaction mechanism was investigated with control experiments and photophysical experiments as well as DFT calculations.
Catalyst free approach to benzimidazoles using air as the oxidant at room temperature
Zhang, Chun,Zhang, Liangren,Jiao, Ning
supporting information, p. 3273 - 3276 (2013/01/16)
A green and practical method to construct benzimidazoles, which are ubiquitous structural units in a number of biologically active compounds, has been developed. The catalyst and additive free conditions, using air as oxidant and the mild conditions make
Homolytic substitution and carbenoidic reactions in the preparation of benzimidazole derivatives of pharmaceutical interest: Synthesis and properties of (2-cycloalkyl-1-benzimidazolyl)-N,N-diethylacetamides
Pellicciari,Fringuelli,Natalini,Brucato,Contessa
, p. 393 - 399 (2007/10/02)
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