Nitrosation and hydrazine derivatives. 7. Reactions of phenelzine, endralazine and procorbazine under nitrosation conditions was written by Hanefeld, Wolfgang;Hunz, Ingrid. And the article was included in Archiv der Pharmazie (Weinheim, Germany) in 1992.Name: 4-Formyl-N-isopropylbenzamide This article mentions the following:
The nitrosation of phenelzine [(2-phenylethyl)hydrazine], endralazine [6-benzoyl-5,6,7,8-tetrahydropyrido[4,3-c]pyridazin-3(2H)-one 3-hydrazone] and procarbazine [N-(1-methylethyl)-4-[(2-methylhydrazino)methyl]benzamide] was investigated and the mechanism was discussed. In the experiment, the researchers used many compounds, for example, 4-Formyl-N-isopropylbenzamide (cas: 13255-50-0Name: 4-Formyl-N-isopropylbenzamide).
4-Formyl-N-isopropylbenzamide (cas: 13255-50-0) belongs to amides. In primary and secondary amides, the presence of N–H dipoles allows amides to function as H-bond donors as well. Thus amides can participate in hydrogen bonding with water and other protic solvents; the oxygen atom can accept hydrogen bonds from water and the N–H hydrogen atoms can donate H-bonds. Amides are stable compounds. The lower-melting members (such as acetamide) can be readily purified by fractional distillation. Most amides are solids which have low solubilities in water.Name: 4-Formyl-N-isopropylbenzamide
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics