• 1. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 2. Evidence of rutile-to-anatase photo-induced electron transfer in mixed-phase TiO2 by solid-state NMR spectroscopy?
  Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
• 3. Exceptional activity of sub-nm Pt clusters on CdS for photocatalytic hydrogen production: a combined experimental and first-principles study?
  Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
• 4. Ester-directed orthogonal dual C–H activation and ortho aryl C–H alkenylation via distal weak coordination?
  Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
• 5. Distinct correlation between (CN2)x units and pores: a low-cost method for predesigned wide range control of micropore size of porous carbon?
  Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966

2-Hydroxy-4-(naphthalen-2-yl)benzonitrile: A Comprehensive Overview

The compound 2-Hydroxy-4-(naphthalen-2-yl)benzonitrile (CAS No. 1261964-01-5) is a fascinating organic molecule with a unique structure and diverse applications. This compound belongs to the class of benzonitriles, which are widely studied for their potential in various fields, including pharmaceuticals, agrochemicals, and materials science. The benzonitrile group in this molecule contributes to its reactivity and versatility, making it a valuable compound in synthetic chemistry.

Recent studies have highlighted the importance of naphthalene derivatives in drug discovery. The presence of the naphthalen-2-yl group in this compound introduces aromaticity and enhances its stability. This structural feature also plays a significant role in its interaction with biological systems, making it a promising candidate for medicinal applications. Researchers have explored the potential of this compound as an antioxidant and anti-inflammatory agent, which are critical properties for developing new therapeutic agents.

The hydroxyl group (-OH) attached to the benzene ring adds another layer of functionality to this compound. This group increases the molecule's polarity and hydrogen bonding capacity, which are essential for its solubility and bioavailability. Recent advancements in computational chemistry have allowed scientists to model the behavior of 2-Hydroxy-4-(naphthalen-2-yl)benzonitrile in different environments, providing deeper insights into its pharmacokinetics and pharmacodynamics.

In terms of synthesis, this compound can be prepared through various methods, including nucleophilic substitution and coupling reactions. The choice of synthesis route depends on the availability of starting materials and the desired purity of the final product. Researchers have optimized these methods to improve yield and reduce costs, making large-scale production feasible.

One of the most exciting developments involving this compound is its application in nanotechnology. The aromaticity and electron-withdrawing properties of benzonitriles make them ideal candidates for constructing functional materials. Scientists have explored the use of 2-Hydroxy-4-(naphthalen-2-yl)benzonitrile in creating self-assembled monolayers and organic semiconductors, which have potential applications in electronics and sensors.

Furthermore, this compound has shown promise in the field of agricultural chemistry. Its ability to act as an effective herbicide has been demonstrated in recent studies, where it was found to inhibit the growth of various weed species without causing significant harm to crops. This property makes it a valuable addition to sustainable agricultural practices.

The environmental impact of 2-Hydroxy-4-(naphthalen-2-yl)benzonitrile has also been a topic of interest. Researchers have investigated its biodegradability and toxicity levels under different conditions. Preliminary results suggest that it is relatively non-toxic to aquatic life, which aligns with current trends toward eco-friendly chemical compounds.

In conclusion, 2-Hydroxy-4-(naphthalen-2-yl)benzonitrile (CAS No. 1261964-01-5) is a multifaceted compound with a wide range of applications across various industries. Its unique structure, functional groups, and reactivity make it a valuable tool in synthetic chemistry and material science. As research continues to uncover new properties and applications, this compound is poised to play an even more significant role in advancing modern science and technology.

• 2492-28-6(2-hydroxy-5-phenylbenzonitrile)
• 594813-05-5(3-Hydroxy-[1,1'-biphenyl]-4-carbonitrile)
• 1261973-55-0(2-Cyano-5-(4-cyanophenyl)phenol)
• 1261973-27-6(2-Cyano-4-(4-hydroxyphenyl)phenol)
• 1261963-33-0(2-Cyano-5-(3-methylphenyl)phenol)
• 253679-12-8(2-hydroxy-5-(4-methylphenyl)benzonitrile)
• 1261973-36-7(2-Cyano-5-(4-hydroxyphenyl)phenol)
• 1261997-99-2(2-Cyano-5-(3-hydroxyphenyl)phenol)
• 1261897-94-2(2-Cyano-5-(3-cyanophenyl)phenol)
• 1261898-00-3(2-hydroxy-5-naphthalen-2-ylbenzonitrile)