62969-86-2 Usage
Description
3-Ethyl-pyridin-2-ol, a derivative of pyridine with the molecular formula C8H9NO, is a chemical compound featuring a hydroxyl group and an ethyl substituent attached to the second carbon atom of the pyridine ring. It is a colorless to light yellow liquid with a faint odor and is recognized for its potential antioxidant and anti-inflammatory properties, as well as its applications in the synthesis of drugs and pesticides.
Uses
Used in Pharmaceutical Industry:
3-Ethyl-pyridin-2-ol is used as a building block for the synthesis of various drugs, contributing to the development of new medicinal compounds due to its unique chemical structure and properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Ethyl-pyridin-2-ol serves as a key component in the creation of pesticides, enhancing crop protection and contributing to increased agricultural productivity.
Used in Antioxidant Applications:
3-Ethyl-pyridin-2-ol is utilized for its potential antioxidant properties, which can help in the prevention of oxidative damage and the mitigation of free radicals, thus playing a role in various health and industrial applications.
Used in Anti-Inflammatory Applications:
Due to its potential anti-inflammatory properties, 3-Ethyl-pyridin-2-ol may be employed in the development of treatments for inflammatory conditions, offering a novel approach to managing such disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 62969-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,6 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62969-86:
(7*6)+(6*2)+(5*9)+(4*6)+(3*9)+(2*8)+(1*6)=172
172 % 10 = 2
So 62969-86-2 is a valid CAS Registry Number.
62969-86-2Relevant articles and documents
Furopyridines. XXXI [1]. Birch reduction of furopyridines
Yamaguchi, Seiji,Hamade, Eriko,Yokoyama, Hajime,Hirai, Yoshiro,Shiotani, Shunsaku
, p. 335 - 339 (2007/10/03)
Birch reduction of four furopyridines 1a-d effected the characteristic cleavage of the furan ring, giving ethnylpyridinols 2a-d, vinylpyridinols 3b,d, and ethylpyridinols 4a-d, and the reduction of the furan ring, giving dihydrofuropyridine 5c,d.
