126474-06-4 Usage
Molecular Structure
1H-Pyrano[4,3-c]pyridine,3,4-dihydro-(9CI) has a complex molecular structure with a heterocyclic ring system containing both pyran and pyridine rings.
Chemical Family
It belongs to the family of pyrano-pyridine compounds and is a derivative of pyridine.
Versatile Reactivity
The compound is known for its versatile reactivity, making it potentially useful in organic chemistry research.
Potential Applications
1H-Pyrano[4,3-c]pyridine,3,4-dihydro-(9CI) has potential applications in drug discovery and development.
Safety Precautions
It is important to handle 1H-Pyrano[4,3-c]pyridine,3,4-dihydro-(9CI) with care and in accordance with proper safety protocols due to its potential toxicity and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 126474-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,7 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 126474-06:
(8*1)+(7*2)+(6*6)+(5*4)+(4*7)+(3*4)+(2*0)+(1*6)=124
124 % 10 = 4
So 126474-06-4 is a valid CAS Registry Number.
126474-06-4Relevant academic research and scientific papers
INTRAMOLECULAR INVERSE ELECTRON DEMAND DIELS-ALDER REACTIONS OF PYRAZINES
Biedrzycki, Marek,Bie, Dick A. de,Plas, Henk C. van der
, p. 6211 - 6220 (2007/10/02)
Thermally induced intramolecular Diels-Alder cyclisations of (alkynyloxyalkyl)pyrazines to dihydropyranopyridines have been studied in the solvent undecane.The introduction of a phenyl group in the α-position of the 3-butynyloxymethyl side chain leads to a 3-4 fold increase of the reaction rate, while the influence of a γ-phenyl group on the rate is negligible.The (3-butynyloxymethyl)pyrazine reacts about 7 times slower than the (3-propynyloxyethyl)pyrazine; the presence of a trimethylsilyl group at the terminus of the alkyne decreases in general the rate of the intramolecular cyclisation.The mechanisms are discussed.
