372147-49-4 Usage
General Description
ETHYL IMIDAZO[1,2-A]PYRIDINE-7-CARBOXYLATE 98 is a chemical compound that is commonly used in the pharmaceutical industry for its potential therapeutic properties. It is a pyridine derivative with an imidazole ring, and its molecular structure and properties make it suitable for use in drug discovery and development. ETHYL IMIDAZO[1,2-A]PYRIDINE-7-CARBOXYLATE 98 may have applications in the treatment of various medical conditions due to its potential pharmacological effects. It is important to handle and use this chemical with care and in compliance with safety regulations, as it may pose health hazards if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 372147-49-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,1,4 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 372147-49:
(8*3)+(7*7)+(6*2)+(5*1)+(4*4)+(3*7)+(2*4)+(1*9)=144
144 % 10 = 4
So 372147-49-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2/c1-2-14-10(13)8-3-5-12-6-4-11-9(12)7-8/h3-7H,2H2,1H3
372147-49-4Relevant articles and documents
Facile synthesis of imidazo[1,2-a]pyridines via tandem reaction
Jia, Jiong,Ge, Yan-Qing,Tao, Xu-Tang,Wang, Jian-Wu
experimental part, p. 185 - 194 (2010/06/14)
An efficient method for the synthesis of 5,6,7-trisubstituted imidazo[1,2-a]pyridines was developed. The products were obtained in good yields under mild conditions.
Heterocyclization of functionalized vinylic derivatives of imidazo[1,2-α]pyridines
Chezal,Moreau,Delmas,Gueiffier,Blache,Grassy,Lartigue,Chavignon,Teulade
, p. 6576 - 6584 (2007/10/03)
Heterocyclization of functionalized vinylic derivatives of imidazo[1,2-α]pyridines was explored experimentally and theoretically using semiempirical AM1 and ab initio methods. A range of functionalized vinylic derivatives (azido, amino, and carbodiimide groups) were prepared for conversion into pyrroloazaindoles 19-22, imidazo[1,x]-; (x=5, 6, 7, 8), [2,6]-, and [2,7]naphthyridines 28-30, 35-38 by thermal reaction. In the case of vinylic groups in the 5 position, peri annulation also was observed. The experimental and theoretical data are compared and discussed.
