25635-17-0 Usage
General Description
2-Methylisonicotinic acid ethyl ester is a chemical compound with the molecular formula C10H11NO2. It is an ester derivative of 2-methylisonicotinic acid, which is a derivative of nicotinic acid. 2 -METHYLISONICOTINIC ACID ETHYL ESTER is commonly used in organic synthesis and pharmaceutical research. It has potential applications in the development of new drugs and medical treatments due to its structural properties and chemical reactivity. 2-Methylisonicotinic acid ethyl ester is known to have various biological activities and is the subject of ongoing research in the fields of chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 25635-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,3 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25635-17:
(7*2)+(6*5)+(5*6)+(4*3)+(3*5)+(2*1)+(1*7)=110
110 % 10 = 0
So 25635-17-0 is a valid CAS Registry Number.
25635-17-0Relevant articles and documents
QUINUCLIDINONE ANALOGUES AS ANTICANCER AGENTS
-
Page/Page column 75-76, (2021/08/13)
The disclosure includes compounds of Formula (I) and Formula(A) wherein R1, R2, R3, m, n, k, and L are defined herein. Also disclosed are methods for treating a neoplastic disease, autoimmune disease, or an inflammatory disorder with these compounds.
Synthesis of Functionalized Pyridines via a Regioselective Oxazoline Promoted C-H Amidation Reaction
Maiden, Tracy M. M.,Swanson, Stephen,Procopiou, Panayiotis A.,Harrity, Joseph P. A.
supporting information, p. 3434 - 3437 (2016/07/26)
The first Rh-catalyzed C-H amidation of pyridines is reported. The incorporation of a substituent at the C2 position both is crucial to the success of this transformation and provides considerable scope for further elaboration of the resulting products. Among these compounds, 2-chloropyridines allow access to a selection of intermediates including a versatile azaquinazoline scaffold.
