15029-44-4 Usage
General Description
2-CYANO-N-(2-METHOXY-ETHYL)-ACETAMIDE, also known as ethyl 2-cyano-2-(2-methoxyethyl)acetamide, is a chemical compound with the molecular formula C8H12N2O2. It is an amide derivative with a cyano group and a 2-methoxyethyl substituent attached to the nitrogen atom. 2-CYANO-N-(2-METHOXY-ETHYL)-ACETAMIDE is used in organic synthesis and medicinal chemistry as a building block and intermediate in the production of various pharmaceuticals and agrochemicals. It also has potential use as a reagent in the preparation of other chemical compounds. Its properties and applications make 2-CYANO-N-(2-METHOXY-ETHYL)-ACETAMIDE a valuable and versatile chemical compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 15029-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,2 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15029-44:
(7*1)+(6*5)+(5*0)+(4*2)+(3*9)+(2*4)+(1*4)=84
84 % 10 = 4
So 15029-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O2/c1-10-5-4-8-6(9)2-3-7/h2,4-5H2,1H3,(H,8,9)
15029-44-4Relevant articles and documents
Cyanoacetamides (IV): Versatile one-pot route to 2-quinoline-3-carboxamides
Wang, Kan,Herdtweck, Eberhardt,Doemling, Alexander
supporting information; scheme or table, p. 316 - 322 (2012/06/18)
Cyanoacetic acid derivatives are the starting materials for a plethora of multicomponent reaction (MCR) scaffolds. Herein, we describe scope of a valuable general protocol for the synthesis of arrays of 2-aminoquinoline-3-carboxamides from cyanoacetamides and 2-aminobenzaldehydes or heterocyclic derivatives via a Friedlaender reaction variation. In many cases, the reactions involve a very convenient work up by simple precipitation and filtration. More than 40 new products are described. We foresee our protocol and the resulting derivatives becoming very valuable to greatly expanding the scaffold space of cyanoacetamide derivatives.
