51984-46-4 Usage
Uses
Used in Organic Synthesis:
(3-Methoxy-pyridin-2-yl)-methanol is used as a chemical intermediate for the synthesis of various organic compounds. Its phenolic alcohol group allows for versatile reactions and modifications, making it a valuable component in the creation of a range of products.
Used in the Production of Phenolic Resins:
In the chemical industry, (3-Methoxy-pyridin-2-yl)-methanol is utilized as a key ingredient in the production of phenolic resins. These resins are known for their heat resistance and are commonly used in the manufacturing of plastics, coatings, and adhesives.
Used in Pharmaceutical Research:
(3-Methoxy-pyridin-2-yl)-methanol is studied for its potential biological activities, including its role as an antioxidant. Its antioxidant properties suggest that it may have applications in the development of pharmaceuticals aimed at combating oxidative stress-related conditions.
Used in Therapeutic Applications:
(3-Methoxy-pyridin-2-yl)-methanol's potential therapeutic applications are being explored, particularly in the context of its biological activities. This may lead to its use in the development of new treatments for various health conditions, leveraging its antioxidant and other biological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 51984-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51984-46:
(7*5)+(6*1)+(5*9)+(4*8)+(3*4)+(2*4)+(1*6)=144
144 % 10 = 4
So 51984-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO2/c1-10-7-3-2-4-8-6(7)5-9/h2-4,9H,5H2,1H3
51984-46-4Relevant academic research and scientific papers
Influence of steric crowding on the electrochemical reduction of substituted tertiary pyridylcarboxamides in aqueous acidic medium
Largeron, Martine,Auzeil, Nicolas,Bacque, Eric,Fleury, Maurice-Bernard
, p. 495 - 501 (2007/10/03)
In order to assess the influence of the steric crowding on the electrochemical reduction of pyridycarboxamides, we have studied a series of tertiary aromatic or alicyclic pyridylcarboxamides. We have shown that increasing steric hindrance at the amide nit
