Bianchi, Maria C. published the artcileSome Aliphatic Cyanoacetylamines, SDS of cas: 15029-36-4, the publication is Atti accad. sci. Torino (1913), 654-9, database is CAplus.
5 cc. CNCH2CO2Et in 35 cc. Et2O + 20 cc. absolute alc. after a passage of an excess of NH3 gave 3 g. NCCH2CONH2, crystals from MeOH, m. 124-5°. 7 g. CNCH2CO2Et in 25 cc. Et2O + 17 cc. absolute alc. and 25 cc. of 20% MeNH2 gave 5 g. of cyanoacetmethylamide, CNCH2CONHMe, m. 104-5°, decompose with KOH, neutralized with HCl its solution becomes yellow. Similarly, the ethylamide, colorless prisms from EtOH, m. 74-50. CNCH2CO2Et (2 mol.) + propylenediamine (1 mol.) gives dicyanoacetopropylenediamide, (CNCH2CONH)2C2H6, m. 161-2°, with KMnO4 gives HCN and the corresponding propyleneoxamic acid. Similarly the trimethylenediamide, CH2(CH2NHCOCH2CN)2, m. 163-5°, decompose 200-10°, giving NH3, gives a neutral H2O solution, gives HCN and the corresponding oxamic acid with KMnO4.
Atti accad. sci. Torino published new progress about 15029-36-4. 15029-36-4 belongs to amides-buliding-blocks, auxiliary class Nitrile,Amine,Aliphatic hydrocarbon chain,Amide, name is 2-Cyano-N-ethylacetamide, and the molecular formula is C5H8N2O, SDS of cas: 15029-36-4.
Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics