• 1. Emulsion technologies for multicellular tumour spheroid radiation assays?
  Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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  Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
• 3. Distinction of trans–cis photoisomers with comparable optical properties in multiple-state photochromic systems – examining a molecule with three azobenzenes via in situ irradiation NMR spectroscopy?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Phenylbutylamines

2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol: A Comprehensive Overview

The compound 2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol (CAS No. 1544945-16-5) is a versatile organic molecule with significant potential in various fields of chemistry and materials science. This compound, characterized by its unique structure, has garnered attention due to its applications in drug discovery, polymer synthesis, and advanced materials development. Recent studies have highlighted its role in enhancing the performance of biodegradable polymers, making it a promising candidate for sustainable materials innovation.

2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol is structurally defined by its hydroxyl group (-OH) at the first carbon, an aminomethyl group (-CH?NH?) at the second carbon, and a 3-bromophenyl group attached to the fourth carbon of a butane chain. This arrangement imparts the molecule with both hydrophilic and hydrophobic properties, which are advantageous in creating amphiphilic materials. The presence of the bromine atom in the aromatic ring further enhances its reactivity and selectivity in various chemical reactions.

Recent research has focused on leveraging 2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol in the development of stimuli-responsive polymers. These polymers can undergo structural changes in response to external stimuli such as temperature, pH, or light, opening new avenues for applications in drug delivery systems and smart materials. For instance, studies have demonstrated that incorporating this compound into polyurethane networks can significantly improve their mechanical properties and biocompatibility.

In addition to its role in polymer science, 2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol has shown promise in medicinal chemistry. Its ability to act as a chelating agent makes it a valuable component in designing metalloenzymes and catalysts for asymmetric synthesis. Recent advancements have also explored its potential as a building block for constructing complex natural product analogs, which could lead to novel therapeutic agents.

The synthesis of 2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol typically involves multi-step organic reactions, including nucleophilic substitution and reduction processes. Researchers have optimized these methods to achieve higher yields and better purity, ensuring scalability for industrial applications.

From an environmental standpoint, 2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol exhibits favorable biodegradation characteristics under controlled conditions, making it a sustainable choice for eco-friendly chemical processes. Its compatibility with enzymatic systems further underscores its potential in green chemistry initiatives.

In conclusion, 2-(Aminomethyl)-4-(3-bromophenyl)butan-1-ol (CAS No. 1544945-16-5) stands out as a multifaceted compound with wide-ranging applications across diverse scientific domains. Its unique chemical properties and recent research breakthroughs position it as a key player in advancing modern materials science and pharmaceutical innovation.

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