1799-79-7 Usage
Uses
Used in Pharmaceutical Industry:
2-(Trifluoromethyl)-5,6-dimethyl-1H-benzimidazole is used as a building block for the synthesis of various pharmaceutical drugs. Its unique structure allows for the development of new drugs with potential antiparasitic, antitumor, and antibacterial activities, making it a promising candidate for drug discovery and development.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(Trifluoromethyl)-5,6-dimethyl-1H-benzimidazole is also utilized as a building block in the synthesis of agrochemicals. Its properties can contribute to the creation of new compounds with pesticidal or herbicidal effects, enhancing crop protection and yield.
Used in Materials Science:
2-(Trifluoromethyl)-5,6-dimethyl-1H-benzimidazole has potential applications in materials science as a stabilizing agent. Its chemical structure can improve the stability and performance of certain materials, making it a valuable component in the development of advanced materials.
Used in Biological Imaging:
As a fluorescent probe, 2-(Trifluoromethyl)-5,6-dimethyl-1H-benzimidazole has potential uses in biological imaging. Its fluorescent properties can be employed to track and visualize biological processes, offering insights into various research areas and diagnostic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1799-79-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1799-79:
(6*1)+(5*7)+(4*9)+(3*9)+(2*7)+(1*9)=127
127 % 10 = 7
So 1799-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F3N2/c1-5-3-7-8(4-6(5)2)15-9(14-7)10(11,12)13/h3-4H,1-2H3,(H,14,15)
1799-79-7Relevant academic research and scientific papers
Bougrin, Khalid,Loupy, André,Petit, Alain,Daou, Boujemaa,Soufiaoui, Mohamed
, p. 163 - 168 (2001)
Cyclocondensation of N-(carbotrifluoromethyl)-ortho-arylenediamines leads to a series of 2-trifluoromethylarylimidazoles with good yields on montmorillonite K10 in 'dry media' under microwave irradiation within 2 min in a domestic oven. By conventional heating in the same conditions, no reaction is observed.
Fe(OTf)3-catalyzed practical synthesis of 2-trifluoromethylarylimidazoles from o-arylenediamines and hexafluoroacetylacetone
Zhou, Yanmei,Shen, Guanshuo,Sui, Yuebo,Zhou, Haifeng
supporting information, p. 3396 - 3399 (2016/07/11)
An iron-catalyzed practical synthesis of 2-trifluoromethylarylimidazoles through condensation of o-arylenediamines and hexafluoroacetylacetone followed by intramolecular addition and C–C bond cleavage in one-pot has been developed. A series of title compounds were obtained with up to 99% yield. This method is quite practical and suitable for scalable preparation due to simple experimental procedure and readily available reagents.
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.
