193481-62-8 Usage
Uses
Used in Organic Synthesis:
2-(dimethylamino)-6-fluoronicotinaldehyde is used as a reagent in organic synthesis for its ability to participate in a variety of chemical reactions, contributing to the formation of complex organic molecules.
Used in Fluorescent Probes for Biomolecular Imaging:
Leveraging its fluorescent properties, 2-(dimethylamino)-6-fluoronicotinaldehyde is used as a component in the development of fluorescent probes. These probes are essential for visualizing and studying biomolecular structures and interactions within biological systems.
Used in Pharmaceutical Development:
2-(dimethylamino)-6-fluoronicotinaldehyde is utilized in the production of various pharmaceuticals due to its potential pharmacological properties. It has been studied for its possible role as an antiviral, anti-inflammatory, and antioxidant agent, indicating its broad-spectrum therapeutic potential.
Used in Agricultural Product Development:
2-(dimethylamino)-6-fluoronicotinaldehyde also finds application in the agricultural sector, where it is used in the development of agricultural products, potentially contributing to crop protection or enhancement of crop characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 193481-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,8 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193481-62:
(8*1)+(7*9)+(6*3)+(5*4)+(4*8)+(3*1)+(2*6)+(1*2)=158
158 % 10 = 8
So 193481-62-8 is a valid CAS Registry Number.
193481-62-8Relevant academic research and scientific papers
The structural proliferation of 2,6-difluoropyridine through organometallic intermediates
Schlosser, Manfred,Rausis, Thierry
, p. 1018 - 1024 (2007/10/03)
Contrary to a literature claim, 2,6-difluoropyridine-3-carboxaldehyde can be readily prepared by consecutive treatment of 2,6-difluoropyridine with lithium diisopropylamide and N,N-dimethylformamide. Regioselective displacements of fluorine from the aldehyde by nucleophiles were carried out. To demonstrate the versatility of the organometallic approach, some two dozens of further 2,6-difluoropyridine derivatives were prepared applying a combination of modern organometallic methods such as site selective hydrogen/metal and halogen/metal permutations and deprotonation-triggered heavy halogen migrations. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
Synthesis of some piperazinylpyrazolo[3,4-b]pyridines as selective serotonin re-uptake inhibitors
Shutske, Gregory M.,Roehr, Joachim E.
, p. 789 - 795 (2007/10/03)
A number of 3-substituted 6-piperazinylpyrazolo[3,4-b]pyridines were synthesized from 2,6-difluoropyridine by directed ortho metallation and sequential intra- and intermolecular displacement of fluorine. Three derivatives with a cyano group in the 3-position showed activity as selective serotonin re-uptake inhibitors.
