58235-52-2 Usage
Chemical class
Flavonoid compound
Natural occurrence
Found in various plants and herbs
Chemical structure
Consists of three methoxy groups and a phenoxy group attached to a central benzene ring
Bioactivity
Natural bioactive compound
Functional groups
Contains methoxy and phenoxy functional groups
Molecular weight
346.32 g/mol (not provided in the material, but can be calculated from the molecular formula)
Physical state
Likely a solid (not provided in the material, but can be inferred from the presence of multiple methoxy groups)
Solubility
Likely soluble in organic solvents and slightly soluble in water (not provided in the material, but can be inferred from the presence of methoxy groups)
Properties
Polyphenolic compound with antioxidant, anti-inflammatory, and anticancer properties
Therapeutic effects
Potential benefits for cardiovascular diseases, neurodegenerative disorders, and cancer
Additional properties
Being investigated for antimicrobial and antiviral properties
Applications
Interest in the development of new pharmaceuticals and dietary supplements due to its various health-promoting properties
Check Digit Verification of cas no
The CAS Registry Mumber 58235-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,3 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58235-52:
(7*5)+(6*8)+(5*2)+(4*3)+(3*5)+(2*5)+(1*2)=132
132 % 10 = 2
So 58235-52-2 is a valid CAS Registry Number.
58235-52-2Relevant academic research and scientific papers
Investigation of the mechanism of action of pyrogallol-phloroglucinol transhydroxylase by using putative intermediates
Paizs, Csaba,Bartlewski-Hof, Ulrike,Rétey, János
, p. 2805 - 2811 (2008/02/05)
Pyrogallol-phloroglucinol transhydroxylase from Pelobacter acidigallici, a molybdopterin-containing enzyme, catalyzes a key reaction in the anaerobic degradation of aromatic compounds. In vitro, the enzymatic reaction requires 1,2,3,5-tetrahydroxy-benzene as a cocatalyst and the trans-hydroxylation occurs without exchange with hydroxy groups from water. To test our previous proposal that the transfer of the hydroxy group occurs via 2,4,6,3′,4′, 5′-hexahydroxydiphenyl ether as an intermediate, we synthesized this compound and investigated its properties. We also describe the synthesis and characterization of 3,4,5,3′,4′,5′-hexahydroxydiphenyl ether. Both compounds could substitute for the cocatalyst in vitro. This indicates that the diphenyl ethers can intrude into the active site and initiate the catalytic cycle. Recently, the X-ray crystal structure of the transhydroxylase (TH) was published[16] and it supports the proposed mechanism of hydroxy-group transfer.
