61893-02-5 Usage
Description
2-Ethyl-3-pyridinol is an organic compound with the chemical formula C7H9NO. It is a white crystalline solid that is soluble in water and has a characteristic pyridine-like odor. 2-Ethyl-3-pyridinol is known for its reactivity and is commonly used as a reagent in various chemical processes.
Uses
Used in Chemical Synthesis:
2-Ethyl-3-pyridinol is used as a reagent in the preparation of 3-hydroxypyridine, which possesses antioxidant properties. This makes it a valuable component in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals that require antioxidant activity for their stability and effectiveness.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Ethyl-3-pyridinol is used as an intermediate in the synthesis of drugs with potential therapeutic applications. Its ability to form stable complexes with metal ions and its antioxidant properties make it a promising candidate for the development of new medications, particularly those targeting metal-related diseases or oxidative stress-related conditions.
Used in Agrochemical Industry:
2-Ethyl-3-pyridinol is also utilized in the agrochemical industry for the development of compounds with pesticidal or herbicidal properties. Its reactivity and ability to form stable complexes can be harnessed to create new agrochemicals that are more effective and environmentally friendly.
Check Digit Verification of cas no
The CAS Registry Mumber 61893-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,9 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61893-02:
(7*6)+(6*1)+(5*8)+(4*9)+(3*3)+(2*0)+(1*2)=135
135 % 10 = 5
So 61893-02-5 is a valid CAS Registry Number.
61893-02-5Relevant 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.
