97465-73-1 Usage
Description
2-[2,6-Dimethoxy-4-[tetrahydro-4-(4-hydroxy-3,5-dimethoxyphenyl)-1H,3H-furo[3,4-c]furan-1-yl]phenoxy]-1-(4-hydroxy-3-methoxyphenyl)-1,3-propanediol is a complex organic compound with a unique structure that features multiple hydroxy and methoxy groups. It belongs to the class of guaiacyl lignins and is a derivative of syringaresinol, with a guaiacylglycerol group replacing one of the phenolic hydrogens. 2-[2,6-Dimethoxy-4-[tetrahydro-4-(4-hydroxy-3,5-dimethoxyphenyl)-1H,3H-furo[3,4-c]furan-1-yl]phenoxy]-1-(4-hydroxy-3-methoxyphenyl)-1,3-propanediol is found in Arabidopsis thaliana, a model organism in plant biology.
Uses
Used in Pharmaceutical Industry:
2-[2,6-Dimethoxy-4-[tetrahydro-4-(4-hydroxy-3,5-dimethoxyphenyl)-1H,3H-furo[3,4-c]furan-1-yl]phenoxy]-1-(4-hydroxy-3-methoxyphenyl)-1,3-propanediol is used as a pharmaceutical compound for its potential therapeutic applications. The presence of multiple hydroxy and methoxy groups allows it to interact with various biological targets and modulate cellular processes. Its specific application and mechanism of action in the pharmaceutical industry need further research and development.
Used in Chemical Research:
2-[2,6-Dimethoxy-4-[tetrahydro-4-(4-hydroxy-3,5-dimethoxyphenyl)-1H,3H-furo[3,4-c]furan-1-yl]phenoxy]-1-(4-hydroxy-3-methoxyphenyl)-1,3-propanediol is used as a research compound in chemical and biological studies. Its unique structure and functional groups make it an interesting subject for investigating the properties and potential applications of complex organic compounds. Researchers can explore its chemical reactivity, interactions with other molecules, and its role in biological systems.
Used in Plant Biology:
2-[2,6-Dimethoxy-4-[tetrahydro-4-(4-hydroxy-3,5-dimethoxyphenyl)-1H,3H-furo[3,4-c]furan-1-yl]phenoxy]-1-(4-hydroxy-3-methoxyphenyl)-1,3-propanediol is found in Arabidopsis thaliana, making it relevant to plant biology research. It can be used to study the biosynthesis, regulation, and function of guaiacyl lignins in plants. Understanding the role of this compound in plant biology can provide insights into the development, growth, and defense mechanisms of plants, as well as their interactions with the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 97465-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,6 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97465-73:
(7*9)+(6*7)+(5*4)+(4*6)+(3*5)+(2*7)+(1*3)=181
181 % 10 = 1
So 97465-73-1 is a valid CAS Registry Number.
97465-73-1Relevant articles and documents
Arabidopsis peroxidase-catalyzed copolymerization of coniferyl and sinapyl alcohols: Kinetics of an endwise process
Demont-Caulet, Nathalie,Lapierre, Catherine,Jouanin, Lise,Baumberger, Stéphanie,Méchin, Valérie
experimental part, p. 1673 - 1683 (2011/02/27)
In order to determine the mechanism of the earlier copolymerization steps of two main lignin precursors, sinapyl (S) alcohol and coniferyl (G) alcohol, microscale in vitro oxidations were carried out with a PRX34 Arabidopsis thaliana peroxidase in the presence of H2O2. This plant peroxidase was found to have an in vitro polymerization activity similar to the commonly used horseradish peroxidase. The selected polymerization conditions lead to a bulk polymerization mechanism when G alcohol was the only phenolic substrate available. In the same conditions, the presence of S alcohol at a 50/50 S/G molar ratio turned this bulk mechanism into an endwise one. A kinetics monitoring (size-exclusion chromatography and liquid chromatography-mass spectrometry) of the different species formed during the first 24 h oxidation of the S/G mixture allowed sequencing the bondings responsible for oligomerization. Whereas G homodimers and GS heterodimers exhibit low reactivity, the SS pinoresinol structure act as a nucleating site of the polymerization through an endwise process. This study is particularly relevant to understand the impact of S units on lignin structure in plants and to identify the key step at which this structure is programmed.
