6342-81-0 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4,6-Tetramethoxybenzoic acid is used as a building block for the synthesis of bioactive molecules due to its unique chemical structure and properties. Its antioxidant and anti-inflammatory characteristics make it a potential candidate for the development of new drugs targeting various health conditions.
Used in Corrosion Inhibition:
2,3,4,6-Tetramethoxybenzoic acid is used as a corrosion inhibitor, leveraging its chemical properties to protect materials from degradation and extending their service life in various industrial applications.
Used in Dyes and Pigments Synthesis:
In the dye and pigment industry, 2,3,4,6-tetramethoxybenzoic acid is used as a component in the synthesis of dyes and pigments, contributing to the development of new colorants with enhanced properties for various applications, including textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 6342-81-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6342-81:
(6*6)+(5*3)+(4*4)+(3*2)+(2*8)+(1*1)=90
90 % 10 = 0
So 6342-81-0 is a valid CAS Registry Number.
6342-81-0Relevant academic research and scientific papers
Synthesis of polyhydroxylated flavonoids bearing a lipophilic decyl tail as potential therapeutic antioxidants
Caldwell, Stuart T.,McPhail, Donald B.,Duthie, Garry G.,Hartley, Richard C.
, p. 23 - 33 (2012/03/07)
Antioxidants have potential for the treatment of stroke and neurodegeneration, and chimeric compounds that combine a flavon-3-ol head group related to myricetin and a lipophilic decyl tail are known to protect membranes from oxidative damage at least as well as vitamin E. New flavon-3-ols that are highly hydroxylated in the B ring in ways not found in natural flavon-3-ols and bearing a lipophilic decyl tail have been prepared from trimethoxy-and tetramethoxybenzoic acids accessed by lithiation-carboxylation reactions. Direct enolate acylation was preferred over Baker-Venkataraman rearrangement when there were methoxy groups at both the 2-and the 6-position of the benzoic acid derivatives.
