((4-Methylphenyl)amino)acetonitrile (CAS 16728-84-0)
((4-Methylphenyl)amino)acetonitrile (CAS:
16728-84-0) has molecular formula C9H10N2 and molecular weight 146.19 g/mol. This compound has been the subject of numerous scientific investigations due to its structural features and practical utility in synthetic chemistry and industrial processes. View product details →
Product Background
This comprehensive research profile examines the scientific literature surrounding ((4-Methylphenyl)amino)acetonitrile.
Key Research Findings
- The biological studies showed a significant interaction of the examined compounds with bovine serum albumin , where the binding constant , Stern-Volmer quenching constant ), and
- Two types of torsional motions, the D-A torsion that results in a nonfluorescent twisted intramolecular charge transfer state and the C horizontal lineC torsion that leads to th
Detailed Literature Analysis
Below are the top-ranked research papers for ((4-Methylphenyl)amino)acetonitrile, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Multifunctional N-substituted 2-pyridylbenzothiazole derivatives: singlet oxygen generation, protein binding, and photoactivated anticancer and antibacterial activities.
This study presents the optical characteristics, and biological characteristics of four N-substituted 2-pyridylbenzothiazole derivatives, namely 6-amino-5-(2-benzothiazolyl)-2-oxo-1-phenyl-1,2-dihydro-3-pyridinecarbonitrile (BTZ-Ph), 6-amino-5-(2-benzothiazolyl)-2-oxo-1-(4-chlorophenyl)-1,2-dihydro-3-pyridinecarbonitrile (BTZ-ClPh), 6-amino-5
2. o-Amino conjugation effect on the photochemistry of trans-aminostilbenes.
The excited-state behavior of a series of trans-2-(N-arylamino)stilbenes (aryl = phenyl (o1H), 4-methylphenyl (o1Me), 4-methoxyphenyl (o1OM), and 4-cyanophenyl (o1CN)) and trans-2-(N,N-diphenylamino)stilbene (o2) in both nonpolar and polar solvents is reported and compared to that of the parent trans-2-aminostilbene and the corresponding meta-
Conclusion
The research literature on ((4-Methylphenyl)amino)acetonitrile demonstrates sustained scientific interest, with publications continuing through 0. The compound serves as an important building block in synthetic chemistry and has been explored for various applications. Researchers and industrial users can view detailed specifications or submit an inquiry for pricing and availability.
Data Sources: PubMed/MEDLINE, CrossRef. 2 papers analyzed. Last updated: 2026-05-25. This article is automatically generated from peer-reviewed research data.