58235-51-1 Usage
Chemical structure
A complex structure containing multiple methoxy groups and a benzene ring.
Molecular weight
368.4 g/mol
Functional groups
Three methoxy groups (-OCH3) attached to the benzene ring and a trimethoxyphenoxy group (-OCH3)3C6H2) attached to the 5th position of the benzene ring.
Physical state
Likely a solid at room temperature due to the presence of multiple methoxy groups.
Solubility
Soluble in organic solvents such as ethanol, methanol, and dichloromethane.
Stability
Stable under normal conditions, but may be sensitive to heat, light, or strong acids and bases.
Synthesis
Commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.
Applications
Potential applications in the development of new drugs and biologically active compounds due to its unique structure and properties.
Organic chemistry
May have uses as a reagent or intermediate in the production of other organic compounds.
Versatility
Important chemical with various potential applications in different industries, such as pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 58235-51-1 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 58235-51:
(7*5)+(6*8)+(5*2)+(4*3)+(3*5)+(2*5)+(1*1)=131
131 % 10 = 1
So 58235-51-1 is a valid CAS Registry Number.
58235-51-1Relevant articles and documents
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.
