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 this compound 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 articles and documents
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.