6742-83-2 Usage
Structure
Benzimidazole derivative with a methyl group and a trifluoromethyl group attached to the nitrogen atom
Potential applications
Pharmaceutical and agrochemical industries as a building block in the synthesis of biologically active compounds, such as antiviral and anticancer agents
Advantages
Unique chemical structure and properties, enhanced chemical and physical properties due to the trifluoromethyl group, useful in designing new materials and drugs
Limitations
Further research needed to fully understand the potential uses and effects in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6742-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6742-83:
(6*6)+(5*7)+(4*4)+(3*2)+(2*8)+(1*3)=112
112 % 10 = 2
So 6742-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3N2/c1-5-3-2-4-6-7(5)14-8(13-6)9(10,11)12/h2-4H,1H3,(H,13,14)
6742-83-2Relevant academic research and scientific papers
Efficient syntheses of 2-fluoroalkylbenzimidazoles and -benzothiazoles
René, Olivier,Souverneva, Alexandra,Magnuson, Steven R.,Fauber, Benjamin P.
supporting information, p. 201 - 204 (2013/02/22)
We report an efficient one-step route to 2-fluoroalkylbenzimidazoles and -benzothiazoles via the condensation of fluorinated carboxylic acids and aromatic diamines or aminothiophenols. Additionally, we describe the syntheses of fluoroalkyl-azabenzimidazoles, -purines, and -imidazolopyrazines. This method is high-yielding with broad scope and is operationally simple with potential application to parallel synthesis.
