Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, European Journal of Organic Chemistry called Exploring the synthetic applicability of a cyanobacterium nitrilase as catalyst for nitrile hydrolysis, Author is Mukherjee, Chandrani; Zhu, Dunming; Biehl, Edward R.; Hua, Ling, which mentions a compound: 17190-29-3, SMILESS is N#CCC(O)C1=CC=CC=C1, Molecular C9H9NO, Related Products of 17190-29-3.
The substrate specificity and synthetic applicability of the nitrilase from cyanobacterium Synechocystis sp. strain PCC 6803 have been examined This nitrilase catalyzed the hydrolysis of both aromatic and aliphatic nitriles to the corresponding acids in high yields. Furthermore, the stereoselective hydrolysis of phenyl-substituted β-hydroxy nitriles to (S)-enriched β-hydroxy carboxylic acids and selective hydrolysis of α,ω-dinitriles with five or less methylene groups to ω-cyano carboxylic acids have been achieved. This suggested that nitrilase from Synechocystis sp. PCC 6803 could be a useful enzyme catalyst for the “”green”” nitrile hydrolysis.
In addition to the literature in the link below, there is a lot of literature about this compound(3-Hydroxy-3-phenylpropanenitrile)Related Products of 17190-29-3, illustrating the importance and wide applicability of this compound(17190-29-3).
Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics