2590-27-4 Usage
Uses
Used in Organic Synthesis:
(3,6-dimethylpyrazin-2-yl)(phenyl)methanol is used as a building block for the synthesis of more complex organic molecules. Its unique structure and potential reactivity make it a valuable component in the creation of new compounds with specific properties.
Used in Pharmaceutical Research:
(3,6-dimethylpyrazin-2-yl)(phenyl)methanol is used as a starting material or intermediate in the development of new pharmaceuticals. Its unique structure may contribute to the discovery of novel drugs with improved efficacy and reduced side effects.
Note: The specific properties and potential applications of (3,6-dimethylpyrazin-2-yl)(phenyl)methanol would need to be further investigated through chemical analysis and testing to fully understand its capabilities and limitations in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2590-27-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2590-27:
(6*2)+(5*5)+(4*9)+(3*0)+(2*2)+(1*7)=84
84 % 10 = 4
So 2590-27-4 is a valid CAS Registry Number.
2590-27-4Relevant academic research and scientific papers
Naphthalene-catalysed lithiation of chlorinated nitrogenated aromatic heterocycles and reaction with electrophiles
Gómez, Inmaculada,Alonso, Emma,Ramón, Diego J.,Yus, Miguel
, p. 4043 - 4052 (2007/10/03)
Naphthalene catalysed reductive lithiation of various chloroazines (1, 7, 10, 13) in the presence of different electrophiles yields, after hydrolysis, the expected functionalised heterocycles with one (2, 8), two (11, 14a-d) and three nitrogen atoms in the ring (14e,f). This methodology allowed us to trap in situ the lithium imine derived from the reaction of 2- pyridyllithium with benzonitrile, by reaction with a Grignard reagent in the presence of titanium alkoxides. 2,4-Dimethoxypyrimidines (14a,c,d) are demethylated under acidic conditions to give the corresponding uracil derivatives 16. (C) 2000 Elsevier Science Ltd.
