• 1. An all-solid-state asymmetric device based on a polyaniline hydrogel for a high energy flexible supercapacitor?
  Hamid Heydari,Mohammad B. Gholivand New J. Chem., 2017,41, 237-244
• 2. An atom efficient route to N-aryl and N-alkyl pyrrolines by transition metal catalysis?
  Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
• 3. An approach for correlating the structural and electrical properties of Zr4+-modified SrBi4Ti4O15/SBT ceramic
  Priyambada Nayak,Tanmaya Badapanda,Anil Kumar Singh,Simanchalo Panigrahi RSC Adv., 2017,7, 16319-16331
• 4. An automatic determination of thoria in thoria-urania mixtures
  Analyst, 1966,91, 208-210
• 5. Alternative donor substrates for inverting and retaining glycosyltransferases?
  Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367

• 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-(Propan-2-yloxy)Pyridin-4-yl]Methanol: A Comprehensive Overview

The compound [2-(propan-2-yloxy)pyridin-4-yl]methanol, identified by the CAS number 754218-88-7, is a versatile organic molecule with significant applications in various fields. This compound has garnered attention in recent years due to its unique structural properties and potential uses in drug development, agrochemicals, and materials science. In this article, we delve into the structural characteristics, physical properties, and latest research findings related to this compound.

The molecular structure of [2-(propan-2-yloxy)pyridin-4-yl]methanol consists of a pyridine ring substituted with an isopropoxy group at the 2-position and a hydroxymethyl group at the 4-position. This arrangement imparts the molecule with a combination of aromatic stability and functional group reactivity, making it a valuable building block in organic synthesis. The SMILES notation for this compound is CC(C)Oc1ncccc1CH2OH, which highlights its structural features. Recent studies have explored the synthesis of this compound through various routes, including nucleophilic substitution and coupling reactions, with a focus on optimizing yield and purity.

From a physical standpoint, [2-(propan-2-yloxy)pyridin-4-yl]methanol exhibits interesting properties that make it suitable for diverse applications. Its molecular weight is approximately 166.19 g/mol, with a melting point around 65°C and a boiling point of 300°C under standard conditions. The compound is sparingly soluble in water but shows good solubility in organic solvents such as dichloromethane and ethyl acetate. These properties have been leveraged in recent research to develop novel drug delivery systems and agrochemical formulations.

In terms of applications, [2-(propan-2-yloxy)pyridin-4-yl]methanol has shown promise in the pharmaceutical industry as an intermediate for synthesizing bioactive compounds. For instance, researchers have utilized this compound as a starting material for developing antiviral agents targeting RNA-dependent RNA polymerase enzymes. Additionally, its pyridine ring has been exploited in the synthesis of herbicides and insecticides, contributing to sustainable agricultural practices.

The latest research on this compound has also explored its role in materials science. By incorporating [2-(propan-2-yloxy strong>)< strong>pyridin strong>-4-yl]< strong>methanol strong>into polymer matrices, scientists have developed advanced materials with enhanced thermal stability and mechanical properties. These materials hold potential for use in high-performance electronics and aerospace applications.

In conclusion, [2-(< strong>propan - 2 - yl oxy strong>)< strong>pyridin strong>-4 - yl ]< strong>methanol strong>, CAS number < strong >754 754 754 754 , is a multifaceted compound with expanding applications across various industries. Its unique structure and favorable physical properties continue to drive innovative research, positioning it as a key player in modern chemical science.

• 52606-06-1(2,6-dimethoxy-4-Pyridinemethanol)
• 156367-50-9(4-Pyridinemethanol, 2-(phenylmethoxy)-)
• 754218-85-4(Pyridine,2-ethoxy-4-[(methoxymethoxy)methyl]-)
• 40864-08-2(2-(Benzyloxy)pyridine)
• 153928-58-6((2-ethoxypyridin-4-yl)methanol)
• 83766-90-9(2-Ethoxy-4-methylpyridine)
• 862507-33-3(2-(propan-2-yloxy)pyridine-4-carboxylic acid)
• 1104461-69-9([6-(propan-2-yloxy)pyridin-3-yl]methanol)
• 123148-66-3((2-Methoxypyridin-4-yl)methanol)
• 57883-15-5(2-(tert-Butoxy)-4-methylpyridine)