51437-32-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-Methyl-5,6-dimethoxybenzimidazole is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the development of new drugs and pesticides.
Used in Anti-inflammatory and Anti-cancer Applications:
2-Methyl-5,6-dimethoxybenzimidazole is used as a potential therapeutic agent for its anti-inflammatory and anti-cancer properties, offering a promising avenue for the treatment of various inflammatory and neoplastic conditions.
Used in Metal Protection Industry:
2-Methyl-5,6-dimethoxybenzimidazole is used as a corrosion inhibitor in metal protection, providing a means to prevent the degradation of metal surfaces and extend the lifespan of metal structures and components.
Safety Considerations:
It is important to handle 2-Methyl-5,6-dimethoxybenzimidazole with care, as exposure to high concentrations can cause irritation to the skin, eyes, and respiratory system, necessitating proper safety measures during its use and manipulation.
Check Digit Verification of cas no
The CAS Registry Mumber 51437-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,3 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51437-32:
(7*5)+(6*1)+(5*4)+(4*3)+(3*7)+(2*3)+(1*2)=102
102 % 10 = 2
So 51437-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O2/c1-6-11-7-4-9(13-2)10(14-3)5-8(7)12-6/h4-5H,1-3H3,(H,11,12)
51437-32-2Relevant academic research and scientific papers
Expanding the aqueous-based redox-facilitated self-polymerization chemistry of catecholamines to 5,6-dihydroxy-1H-benzimidazole and its 2-substituted derivatives
Fan, Ka Wai,Peterson, Matthew B.,Ellersdorfer, Peter,Granville, Anthony M.
, p. 25203 - 25214 (2016/03/22)
Aqueous-base redox-facilitated self-polymerization can be performed with 5,6-dihydroxy-1H-benzimidazole (DHBI) to generate polymeric material that is analogous to poly(dopamine) (PDA), proving the possibility to expand the catecholamine-exclusive chemistr
