297132-89-9 Usage
Uses
Used in Pharmaceutical Industry:
Benzaldehyde, 3-methoxy-4,5-bis(methoxymethoxy)-, is used as a key intermediate in the synthesis of Silybin analogs, which are known for their antioxidant properties. These analogs can be employed in the development of pharmaceuticals targeting various health conditions, including those related to oxidative stress and inflammation.
Used in Chemical Synthesis:
In the field of chemical synthesis, Benzaldehyde, 3-methoxy-4,5-bis(methoxymethoxy)-, can be utilized as a building block for creating a wide range of complex organic molecules. Its unique structure and functional groups make it a valuable component in the synthesis of various compounds with potential applications in different industries, such as pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
Benzaldehyde, 3-methoxy-4,5-bis(methoxymethoxy)-, can also be used in research and development settings to study its chemical properties, reactivity, and potential applications in various fields. Researchers can explore its use in the development of new materials, pharmaceuticals, and other products by understanding its interactions with other molecules and its potential to form new compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 297132-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,3 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 297132-89:
(8*2)+(7*9)+(6*7)+(5*1)+(4*3)+(3*2)+(2*8)+(1*9)=169
169 % 10 = 9
So 297132-89-9 is a valid CAS Registry Number.
297132-89-9Relevant academic research and scientific papers
Guz, Nathan R.,Stermitz, Frank R.
, p. 1140 - 1145 (2000)
Flavonolignans represent natural compounds whose biosynthesis presumes a radical coupling of a ring B catecholic flavonoid with a molecule of coniferyl alcohol or an analogue. Many natural flavonolignans can exist as regioisomers, depending on how the coupled coniferyl alcohol moiety orients to the flavonoid. These regioisomers are often difficult to separate and have virtually identical NMR spectra. Structural assignments for some have changed with time or have been given without proof. We here report syntheses of both regioisomers of the flavonolignan hydnocarpin and one isomer of a plant isolate previously known as 5'-methoxyhydnocarpin. This isomer, here renamed 5'-methoxyhydnocarpin-D, was recently shown to be a potent inhibitor of a Staphylococcus aureus multidrug resistant efflux pump.
