5467-95-8 Usage
Uses
Used in Pharmaceutical Synthesis:
(2,6-dichlorophenyl)(quinolin-2-yl)methanol is used as a key building block for the synthesis of various pharmaceuticals and organic compounds. Its unique structural properties contribute to the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2,6-dichlorophenyl)(quinolin-2-yl)methanol is used as a precursor in the creation of molecules with potential biological activity. Its incorporation into drug candidates can lead to the discovery of novel treatments and medications.
Used in Drug Development:
(2,6-dichlorophenyl)(quinolin-2-yl)methanol plays a role in drug development, where it may be used to construct compounds with specific therapeutic targets. Its potential applications in this area highlight its importance in advancing pharmaceutical research and innovation.
It is important to handle (2,6-dichlorophenyl)(quinolin-2-yl)methanol with care, as it may possess toxic or hazardous properties. Proper safety measures should be taken during its use to minimize any potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 5467-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5467-95:
(6*5)+(5*4)+(4*6)+(3*7)+(2*9)+(1*5)=118
118 % 10 = 8
So 5467-95-8 is a valid CAS Registry Number.
5467-95-8Relevant academic research and scientific papers
From Pyridine- N-oxides to 2-Functionalized Pyridines through Pyridyl Phosphonium Salts: An Umpolung Strategy
Bugaenko, Dmitry I.,Yurovskaya, Marina A.,Karchava, Alexander V.
, p. 6099 - 6104 (2021/08/03)
The reactions of pyridine-N-oxides with Ph3P under the developed conditions provide an unprecedented route to (pyridine-2-yl)phosphonium salts. Upon activation with DABCO, these salts readily serve as functionalized 2-pyridyl nucleophile equivalents. This umpolung strategy allows for the selective C2 functionalization of the pyridine ring with electrophiles, avoiding the generation and use of unstable organometallic reagents. The protocol operates at ambient temperature and tolerates sensitive functional groups, enabling the synthesis of otherwise challenging compounds.
