122509-29-9 Usage
General Description
2,3,6-Tricarboethoxypyridine is a chemical compound with the molecular formula C13H15NO4. It is commonly used as a reagent in organic synthesis, particularly in the preparation of pyridine derivatives. 2,3,6-Tricarboethoxypyridine is a clear, colorless liquid with a slightly sweet odor, and it is soluble in organic solvents. It is often used as a building block in the production of pharmaceutical compounds and agrochemicals. 2,3,6-Tricarboethoxypyridine is also known for its ability to form stable complexes with transition metal ions, making it useful in coordination chemistry. However, it is important to handle this compound with care as it is flammable and may cause irritation to the eyes and skin.
Check Digit Verification of cas no
The CAS Registry Mumber 122509-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,0 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122509-29:
(8*1)+(7*2)+(6*2)+(5*5)+(4*0)+(3*9)+(2*2)+(1*9)=99
99 % 10 = 9
So 122509-29-9 is a valid CAS Registry Number.
122509-29-9Relevant articles and documents
Cp*RuCl-catalyzed [2 + 2 + 2] cycloadditions of α,ω- diynes with electron-deficient carbon-heteroatom multiple bonds leading to heterocycles
Yamamoto, Yoshihiko,Kinpara, Keisuke,Saigoku, Tomoaki,Takagishi, Hideyuki,Okuda, Satoshi,Nishiyama, Hisao,Itoh, Kenji
, p. 605 - 613 (2005)
In the presence of a catalytic amount of Cp*RuCl(cod), 1,6-diynes were allowed to react chemoand regioselectively with electron-deficient nitriles and heterocumulenes at 60-90°C to afford heterocyclic compounds. The mechanism of the ruthenium-catalyzed regioselective formations of bicyclic pyridines and pyridones were analyzed on the basis of density functional calculations. Cyclocotrimerizations of ethyl propiolate with ethyl cyanoformate or propyl isocyanate gave rise to two of the four possible pyridine or pyridone regioisomers.
Preparation and inverse-electron-demand diels-alder reaction of an electron-deficient heterocyclic azadiene: Triethyl 1,2,4-triazine-3,5,6-tricarboxylate and 2,3,6-tricarboethoxypyridine
Boger, Dale L.,Panek, James S.,Yasuda, Masami
, p. 142 - 142 (2017/05/20)
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