33631-05-9 Usage
Description
2-Aminopyridin-4-ol is an organic compound with the molecular formula C5H6N2O. It is a white crystalline solid and is used as an important intermediate in various fields due to its unique chemical properties.
Uses
Used in Organic Synthesis:
2-Aminopyridin-4-ol is used as a key intermediate for the synthesis of various organic compounds. Its presence in the molecule allows for further functionalization and the creation of a wide range of products.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Aminopyridin-4-ol is used as a vital intermediate for the development of new pesticides and other agricultural chemicals. Its unique structure contributes to the effectiveness of these products in controlling pests and diseases.
Used in Pharmaceutical Industry:
2-Aminopyridin-4-ol is employed as a crucial intermediate in the pharmaceutical industry for the synthesis of various drugs. Its versatile chemical properties enable the development of new therapeutic agents with potential applications in treating different medical conditions.
Used in Dyestuff Field:
2-Aminopyridin-4-ol is used as an essential intermediate for the production of dyes and pigments in the dyestuff industry. Its incorporation into dye molecules enhances their color properties and stability, leading to improved performance in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 33631-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,3 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33631-05:
(7*3)+(6*3)+(5*6)+(4*3)+(3*1)+(2*0)+(1*5)=89
89 % 10 = 9
So 33631-05-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O/c6-5-3-4(8)1-2-7-5/h1-3H,(H3,6,7,8)
33631-05-9Relevant articles and documents
Chemoselective Demethylation of Methoxypyridine
Makino, Kosho,Hasegawa, Yumi,Inoue, Takahide,Araki, Koji,Tabata, Hidetsugu,Oshitari, Tetsuta,Ito, Kiyomi,Natsugari, Hideaki,Takahashi, Hideyo
, p. 951 - 954 (2019/05/10)
A chemoselective demethylation method for various methoxypyridine derivatives has been developed. Treatment of 4-methoxypyridine with L-selectride in THF for 2 h at reflux temperature afforded 4-hydroxypyridine in good yield; no reaction to anisole occurred. The utility of our method was demonstrated by the efficient synthesis of the metabolic substances of the antiulcer agent omeprazole. Chemoselective demethylation at the site of 3,5-dimethyl-4-methoxypyridine in the presence of 4-methoxybenzimidazole was achieved.
Improved procedures for preparation of 4-hydroxy- and 2-amemo-4-methoxy-2-aminopyridines
Sundberg, Richard J.,Jiang, Songchun
, p. 117 - 122 (2007/10/03)
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