959855-49-3 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-methoxyphenyl)-2,6-dimethyl-1H-benzimidazole is used as a building block for the synthesis of various drugs and bioactive compounds due to its versatile chemical structure and potential therapeutic properties.
Used in Anti-inflammatory Applications:
1-(4-methoxyphenyl)-2,6-dimethyl-1H-benzimidazole is used as an anti-inflammatory agent for its potential to modulate inflammatory pathways and alleviate inflammation-related conditions.
Used in Anti-cancer Applications:
1-(4-methoxyphenyl)-2,6-dimethyl-1H-benzimidazole is used as an anti-cancer agent, particularly for its potential to target and inhibit cancer cell growth and proliferation.
Used in Anti-microbial Applications:
1-(4-methoxyphenyl)-2,6-dimethyl-1H-benzimidazole is used as an anti-microbial agent for its potential to inhibit the growth of harmful microorganisms, including bacteria and fungi.
Used in Corrosion Inhibition:
1-(4-methoxyphenyl)-2,6-dimethyl-1H-benzimidazole is used as a corrosion inhibitor to protect metals from degradation and extend their service life in various industrial applications.
Used in Biochemical Research:
1-(4-methoxyphenyl)-2,6-dimethyl-1H-benzimidazole is used as a fluorescent probe in biochemical research, allowing for the detection and analysis of specific biological processes and interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 959855-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,8,5 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 959855-49:
(8*9)+(7*5)+(6*9)+(5*8)+(4*5)+(3*5)+(2*4)+(1*9)=253
253 % 10 = 3
So 959855-49-3 is a valid CAS Registry Number.
959855-49-3Relevant academic research and scientific papers
Reactivity-controlled regioselectivity: A regiospecific synthesis of 1,2-disubstituted benzimidazoles
Deng, Xiaohu,Mani, Neelakandha S.
experimental part, p. 680 - 686 (2010/03/04)
We demonstrate exceptional levels of regioselectivity in the tandem, animation reactions between 1,2-differentiated dihaloarenes and N-substituted amidines, The regiochemical outcome of this Cul-catalyzed reaction is achieved through a combination of N1/N2 chemoselectivity on the amidine and reactivity-controlled X1/X2 chemoselectivity on the 1,2-dihaloarene. This reaction proves to be fairly general for the regiospecific synthesis of 1,2-substituted benzimidazoles.
A palladium-catalyzed regiospecific synthesis of N-aryl benzimidazoles
Zheng, Nan,Anderson, Kevin W.,Huang, Xiaohua,Nguyen, Hanh Nho,Buchwald, Stephen L.
, p. 7509 - 7512 (2008/09/17)
(Chemical Equation Presented) Highly tolerated: A catalytic method employing [Pd2(dba)3] and XPhos or RuPhos permits the efficient synthesis of N-aryl benzimidazoles in regioisomerically pure form starting from ortho-halo-anilides (see scheme), and tolerates a wide range of functional groups, dba = trans,trans-dibenzylideneacetone.
