193481-62-8 Usage
General Description
2-(dimethylamino)-6-fluoronicotinaldehyde is a chemical compound with the molecular formula C10H11FN2O. It is a yellow solid that is commonly used as a reagent in organic synthesis. 2-(dimethylamino)-6-fluoronicotinaldehyde is also known for its fluorescent properties and has been used in the development of fluorescent probes for biomolecular imaging. Additionally, it has been studied for its potential pharmacological properties, including its possible role as a potential antiviral, anti-inflammatory, and antioxidant agent. The compound is also used in the production of various pharmaceuticals and agricultural products. Overall, 2-(dimethylamino)-6-fluoronicotinaldehyde has a diverse range of applications and is an important compound in the field of organic chemistry and drug development.
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 articles and documents
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.
