150626-26-9 Usage
Uses
Used in Pharmaceutical Industry:
2,3,6-Trimethoxy-4-methylphenol is used as an antifungal and antibacterial agent for its ability to inhibit the growth of fungi and bacteria, making it a valuable component in the formulation of pharmaceutical products aimed at treating infections.
Used in Cosmetic Industry:
In the cosmetic industry, 2,3,6-Trimethoxy-4-methylphenol is used as a preservative to prevent the growth of microorganisms in products, ensuring their safety and longevity.
Used in Antioxidant Applications:
2,3,6-Trimethoxy-4-methylphenol is used as an antioxidant to protect cells and tissues from oxidative damage, which is a significant factor in the aging process and various diseases.
Used in Cancer Research:
2,3,6-Trimethoxy-4-methylphenol is used as a potential anti-cancer agent due to its ability to inhibit the growth of cancer cells, making it a subject of interest in the development of new cancer therapies.
Used in Chemical Synthesis:
2,3,6-Trimethoxy-4-methylphenol is used as a precursor in the synthesis of various organic compounds, highlighting its importance in the chemical industry for the production of a wide range of products.
Check Digit Verification of cas no
The CAS Registry Mumber 150626-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,2 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150626-26:
(8*1)+(7*5)+(6*0)+(5*6)+(4*2)+(3*6)+(2*2)+(1*6)=109
109 % 10 = 9
So 150626-26-9 is a valid CAS Registry Number.
150626-26-9Relevant academic research and scientific papers
A new fluorogenic transformation: Development of an optical probe for coenzyme Q
Tremblay, Matthew S.,Sames, Dalibor
, p. 2417 - 2420 (2007/10/03)
(Chemical Equation Presented) A new fluorogenic transformation based on a quinone reduction/lactonization sequence has been developed and evaluated as a tool for probing redox phenomena in a biochemical context. The probe presented herein is an irreversible redox probe and is reduced selectively by biologically relevant quinols such as ubiquinol but is inert to reduced nicotinamides (e.g., NADH). The ensuing cyclization is fast and quantitative and provides a measurable optical response.
