6761-87-1 Usage
Uses
Used in Pharmaceutical Industry:
2-Benzimidazolemethanol, alpha, 5,6-trimethyl-(7CI,8CI) is used as a pharmaceutical intermediate for the synthesis of various drugs and active pharmaceutical ingredients. Its unique structure and reactivity may contribute to the development of new therapeutic agents with specific biological activities.
Used in Agricultural Industry:
In the agricultural sector, 2-Benzimidazolemethanol, alpha, 5,6-trimethyl-(7CI,8CI) may be utilized as a chemical component in the formulation of agrochemicals, such as pesticides or plant growth regulators, due to its potential interaction with biological systems at the molecular level.
Used in Materials Science:
2-Benzimidazolemethanol, alpha, 5,6-trimethyl-(7CI,8CI) could be employed in the development of novel materials with specific properties, such as in the creation of advanced polymers, coatings, or composites, where its chemical structure may impart unique characteristics to the final product.
Check Digit Verification of cas no
The CAS Registry Mumber 6761-87-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,6 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6761-87:
(6*6)+(5*7)+(4*6)+(3*1)+(2*8)+(1*7)=121
121 % 10 = 1
So 6761-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O/c1-6-4-9-10(5-7(6)2)13-11(12-9)8(3)14/h4-5,8,14H,1-3H3,(H,12,13)
6761-87-1Relevant academic research and scientific papers
The synthesis, characterization and optical properties of novel pyrido[1,2-a]benzimidazole derivatives
Ge, Yan Qing,Jia, Jiong,Yang, He,Tao, Xu Tang,Wang, Jian Wu
scheme or table, p. 344 - 349 (2011/06/11)
A series of novel, substituted, pyrido[1,2-a]benzimidazole derivatives were synthesized using a novel tandem annulation reaction between 2-acylbenzimidazole derivatives and 4-bromobut-2-enoic esters under mild conditions. The compounds were characterized using IR, 1H NMR, 13C NMR and HRMS; the crystal structure of 2,7,8-trimethyl-3- ethoxycarbonyl-4-phenylpyrido[1,2-a]benzimidazole was determined as orthorhombic. The absorbance and fluorescence spectra of the pyrido[1,2-a]benzimidazoles were measured in dichloromethane; an intense absorption maxima was observed at 250 nm and emission maxima were noted at 460 nm. The absorption spectra and fluorescence characteristics of the pyrido[1,2-a]benzimidazole derivatives revealed that a phenyl and a methyl group attached to the pyrido[1,2-a]benzimidazole ring markedly influenced maximum emission.
