847664-65-7 Usage
Uses
Used in Chemical Synthesis:
2,5-Dichloro-4-hydroxypyridine is used as a reagent or intermediate for the synthesis of various chemical compounds. Its unique structure, which includes two chlorine atoms and a hydroxyl group on a pyridine ring, makes it a valuable component in the creation of a wide range of molecules for different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-Dichloro-4-hydroxypyridine is used as a building block for the development of new drugs. Its chemical properties allow it to be incorporated into the structures of potential therapeutic agents, contributing to the advancement of medicinal chemistry.
Used in Research and Development:
2,5-Dichloro-4-hydroxypyridine is also utilized in research and development settings, where it may be employed to study the properties and reactions of phenylpyridine derivatives. This can lead to a better understanding of their potential applications and the discovery of new compounds with desired characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 847664-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,6,6 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 847664-65:
(8*8)+(7*4)+(6*7)+(5*6)+(4*6)+(3*4)+(2*6)+(1*5)=217
217 % 10 = 7
So 847664-65-7 is a valid CAS Registry Number.
847664-65-7Relevant academic research and scientific papers
Voisin, Anne Sophie,Bouillon, Alexandre,Lancelot, Jean-Charles,Rault, Sylvain
, p. 1417 - 1421 (2005)
This paper describes a general method for the synthesis of halohydroxypyridines from novel halopyridinylboronic acids and esters recently described by some of us. Halopyridinylboronic acids and esters have been efficiently hydroxydeboronated under mild conditions by employing hydrogen peroxide or meta-chloroperbenzoic acid. These hydroxylations take place regioselectively without other oxidation (N-oxide formation).
