• 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
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  Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
• 3. Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices
  Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
• 4. Excitation energies from ground-state density-functionals by means of generator coordinates
  A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
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• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Alkyl aryl ethers
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Ethers Alkyl aryl ethers

2-(Chloromethyl)-5-methoxypyridine: A Comprehensive Overview

2-(Chloromethyl)-5-methoxypyridine (CAS No. 75342-33-5) is a versatile organic compound with significant applications in various fields, including pharmaceuticals, agrochemicals, and materials science. This compound, characterized by its pyridine ring structure with a chloromethyl group at position 2 and a methoxy group at position 5, has garnered attention due to its unique chemical properties and potential for further functionalization.

The chemical properties of 2-(Chloromethyl)-5-methoxypyridine make it an ideal candidate for use in synthesizing bioactive molecules. Recent studies have highlighted its role as an intermediate in the development of novel pesticides and antimicrobial agents. Its ability to undergo nucleophilic substitution reactions, particularly at the chloromethyl group, facilitates the incorporation of diverse functional groups, thereby expanding its utility in drug discovery.

From a synthesis standpoint, researchers have explored various methods to optimize the production of 2-(Chloromethyl)-5-methoxypyridine. Traditional approaches involve the chlorination of pyridine derivatives, followed by alkylation to introduce the methoxy group. However, recent advancements have focused on green chemistry principles, such as using microwave-assisted synthesis or catalytic systems to enhance reaction efficiency and reduce environmental impact.

The application of 2-(Chloromethyl)-5-methoxypyridine extends beyond traditional chemical synthesis. In the field of materials science, it has been utilized as a building block for constructing advanced materials with tailored electronic properties. For instance, its incorporation into polymer frameworks has shown promise in enhancing conductivity and stability, making it a valuable component in the development of next-generation electronic devices.

Recent research has also delved into the biological activity of 2-(Chloromethyl)-5-methoxypyridine, particularly its potential as an anticancer agent. Studies conducted on cellular models have demonstrated its ability to inhibit specific enzymes involved in tumor progression, suggesting a potential pathway for therapeutic intervention.

In conclusion, 2-(Chloromethyl)-5-methoxypyridine (CAS No. 75342-33-5) stands out as a multifaceted compound with vast untapped potential across various industries. Its chemical versatility, combined with ongoing research into novel applications and synthesis methods, underscores its importance in contemporary scientific exploration.

• 55270-47-8(5-Methoxy-2-methylpyridine)
• 62734-08-1(2-(Chloromethyl)-4-methoxypyridine hydrochloride)
• 60617-60-9(2-(chloromethyl)-3-methoxy-pyridine hydrochloride)
• 120870-79-3(2-(Chloromethyl)-5-methoxypyridine)
• 62734-04-7(Pyridine, 2-(chloromethyl)-3-ethoxy-, hydrochloride)
• 80322-74-3(2-(chloromethyl)pyridin-3-ol hydrochloride)
• 159996-13-1(Pyridine,2-(chloromethyl)-4-ethoxy-)
• 127590-89-0(Pyridine,2-(chloromethyl)-5-propoxy-)
• 743375-99-7(2-(chloromethyl)pyridin-3-ol)
• 99651-28-2(2-(Chloromethyl)-4-methoxypyridine)