1547-29-1 Usage
Uses
Used in Pharmaceutical Research and Development:
3-FLUORO-2-HYDROXYPYRIDINE is utilized as a key building block in the synthesis of pharmaceutical drugs. Its unique structure and reactivity contribute to the development of new drug candidates with potential therapeutic applications.
Used in Agrochemical Research and Development:
In the agrochemical industry, 3-FLUORO-2-HYDROXYPYRIDINE serves as an important intermediate for the synthesis of agrochemicals. Its properties enable the creation of novel compounds with applications in crop protection and pest control.
Used in Materials Science:
3-FLUORO-2-HYDROXYPYRIDINE is also employed as an intermediate in the production of fine chemicals and specialty materials. Its unique chemical characteristics allow for the development of advanced materials with specific properties for use in various applications.
Used in Organic Synthesis:
3-FLUORO-2-HYDROXYPYRIDINE plays a crucial role in organic synthesis, where it is used to construct complex organic molecules. Its versatility and reactivity make it a valuable component in the synthesis of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1547-29-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1547-29:
(6*1)+(5*5)+(4*4)+(3*7)+(2*2)+(1*9)=81
81 % 10 = 1
So 1547-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H4FNO/c6-4-2-1-3-7-5(4)8/h1-3H,(H,7,8)
1547-29-1Relevant academic research and scientific papers
OXYGENATION OF THE UNACTIVATED PYRIDINE SYSTEM BY ACETYL HYPOFLUORITE MADE DIRECTLY FROM F2
Rozen, Shlomo,Hebel, David
, p. 249 - 258 (2007/10/02)
Acetyl hypofluorite was found capable of activating the usually unreactive pyridine by substituting the hydrogen at the 2 position by an acetoxy group which then was hydrolyzed to the corresponding pyridinone.Substitutents at 3, 4 or 5 position do not interfere with the reaction, but compounds with substituents at 2 (with the exception of aromatic ones) either do not react or produce tars.The reaction conditions are very mild and the yields are very good for this kind of substitution.Quinolines and pyrazines also react very satisfactorily.
