122637-38-1 Usage
General Description
6-(2-Methyl-1,3-dioxolan-2-yl)-2-pyridinecarboxylic acid is a synthetic compound with potential pharmaceutical applications. It contains a pyridine ring and a carboxylic acid group, making it a potentially useful intermediate in drug synthesis. The presence of the dioxolane ring in the molecule suggests potential for solubility and bioavailability in drug formulations. Additionally, the methyl group on the dioxolane ring provides steric hindrance, which can impact the compound's interactions with biological targets. Overall, this compound may have uses in medicinal chemistry and drug development due to its structural features and potential activity.
Check Digit Verification of cas no
The CAS Registry Mumber 122637-38-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,6,3 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 122637-38:
(8*1)+(7*2)+(6*2)+(5*6)+(4*3)+(3*7)+(2*3)+(1*8)=111
111 % 10 = 1
So 122637-38-1 is a valid CAS Registry Number.
122637-38-1Relevant articles and documents
Linkage isomerism in transition-metal complexes of mixed (arylcarboxamido)(arylimino)pyridine ligands
Boyce, David W.,Salmon, Debra J.,Tolman, William B.
supporting information, p. 5788 - 5796 (2014/06/23)
The synthesis of a series of asymmetric mixed 2,6-disubstituted (arylcarboxamido)(arylimino)pyridine ligands and their coordination chemistry toward a series of divalent first-row transition metals (Cu, Co, and Zn) have been explored. Complexes featuring both anionic N,N,N″-carboxamido and neutral O,N,N-carboxamide coordination have been prepared and characterized by X-ray crystallography, cyclic voltammetry, and UV-visible and EPR spectroscopy. Specifically, RLM(X) (M = Cu; X = Cl-, OAc-) and RL(H)MX2 (M = Cu, Co, Zn; X = Cl-, SbF 6-) complexes that feature N,N,N″- or O,N,N-coordination are presented. Base-induced linkage isomerization from O,N,N-carboxamide to N,N,N″-carboxamido coordination is also confirmed by multiple forms of spectroscopy.
