1122-43-6 Usage
Uses
Used in Pharmaceutical Synthesis:
2,6-DIMETHYL-3-HYDROXYPYRIDINE is used as a key intermediate in the synthesis of pharmaceutical drugs, leveraging its unique structure to contribute to the development of new medications.
Used in Agrochemical Production:
2,6-DIMETHYL-3-HYDROXYPYRIDINE also serves as an intermediate in the production of agrochemicals, playing a crucial role in the creation of substances that protect crops and enhance agricultural productivity.
Used in Organic Compounds Production:
2,6-DIMETHYL-3-HYDROXYPYRIDINE is utilized as an intermediate for the production of a variety of organic compounds, highlighting its versatility in organic chemistry.
Used in Biological and Pharmacological Research:
2,6-DIMETHYL-3-HYDROXYPYRIDINE is used as a subject of study in biological and pharmacological research for its potential antioxidant and neuroprotective effects, which could lead to advancements in medical treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 1122-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1122-43:
(6*1)+(5*1)+(4*2)+(3*2)+(2*4)+(1*3)=36
36 % 10 = 6
So 1122-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO/c1-5-3-4-7(9)6(2)8-5/h3-4,9H,1-2H3
1122-43-6Relevant academic research and scientific papers
Metal-free decarboxylative Hetero-Diels-Alder synthesis of 3-hydroxypyridines: A rapid access to N-fused bicyclic hydroxypiperidine scaffolds
Jouanno, Laurie-Anne,Di Mascio, Vincent,Tognetti, Vincent,Joubert, Laurent,Sabot, Cyrille,Renard, Pierre-Yves
, p. 1303 - 1319 (2014/03/21)
A complete experimental and theoretical study of the thermally controlled metal-free decarboxylative hetero-Diels-Alder (HDA) reaction of 5-alkoxyoxazoles with acrylic acid is reported. This strategy offers a new entry to valuable 2,6-difunctionalized 3-hydroxypyridines from readily available 2- and 4-disubstituted 5-alkoxyoxazoles. The reaction conditions proved compatible with, among others, ketone, amide, ester, ether, and nitrile groups. The broad functional group tolerance of the protocol allows a rapid and versatile access to both hydroxyindolizidine and hydroxyquinolizidine derivatives via a pyridine dearomatization strategy.
