• 1. Excitonic channels from bio-inspired templated supramolecular assembly of J-aggregate nanowires?
  Daniel Messmer,Stefan Salentinig,Jakob Heier Nanoscale, 2019,11, 6929-6938
• 2. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
• 3. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640
• 4. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
• 5. Distributed research: a new paradigm for undergraduate research and global problem solving?
  Bruce Parkinson Energy Environ. Sci., 2010,3, 509-511

Comprehensive Overview of 3-(Cyclopropylmethoxy)benzaldehyde (CAS No. 58986-61-1)

3-(Cyclopropylmethoxy)benzaldehyde (CAS No. 58986-61-1) is a specialized organic compound widely utilized in pharmaceutical and agrochemical research. Its unique molecular structure, featuring a cyclopropylmethoxy group attached to a benzaldehyde core, makes it a valuable intermediate in synthetic chemistry. This compound is particularly relevant in the development of novel bioactive molecules, aligning with current trends in drug discovery and sustainable agriculture.

The growing demand for 3-(Cyclopropylmethoxy)benzaldehyde is driven by its role in synthesizing heterocyclic compounds, which are pivotal in modern medicinal chemistry. Researchers frequently search for "synthesis methods for 3-(Cyclopropylmethoxy)benzaldehyde" or "applications of benzaldehyde derivatives," reflecting its importance in academic and industrial settings. Its stability and reactivity under mild conditions further enhance its appeal for green chemistry applications, a hot topic in 2024.

From a structural perspective, the cyclopropyl ring in 3-(Cyclopropylmethoxy)benzaldehyde introduces steric and electronic effects that influence its reactivity. This characteristic is often explored in studies related to "structure-activity relationships (SAR)" or "small molecule drug design." The compound’s aldehyde functionality also allows for diverse derivatization, making it a versatile building block for high-value fine chemicals.

In the context of AI-assisted drug discovery, 3-(Cyclopropylmethoxy)benzaldehyde has gained attention as a fragment library component. Computational chemists frequently query "benzaldehyde derivatives for virtual screening" or "cyclopropyl-containing pharmacophores," highlighting its relevance in machine learning-driven research. Its compatibility with automated synthesis platforms further positions it as a future-proof reagent.

Environmental and regulatory considerations are also critical when discussing 58986-61-1. The compound’s biodegradability and low ecotoxicity profile align with the EPA’s Safer Choice Program criteria, a trending search topic among sustainability-focused manufacturers. Analytical methods like HPLC purity testing and GC-MS characterization are commonly associated with this compound, ensuring compliance with Good Manufacturing Practices (GMP).

Market analysts note increased procurement of 3-(Cyclopropylmethoxy)benzaldehyde by contract research organizations (CROs), particularly for kinase inhibitor development. This trend correlates with rising searches for "custom synthesis of aromatic aldehydes" and "scalable routes for CAS 58986-61-1." The compound’s cost-effectiveness compared to similar ortho-substituted benzaldehydes adds to its commercial viability.

In material science, derivatives of 3-(Cyclopropylmethoxy)benzaldehyde show promise in organic electronics, especially for OLED precursor synthesis. Recent patents disclose its use in liquid crystal formulations, sparking queries like "benzaldehyde-based dielectric materials." These applications demonstrate its cross-disciplinary utility beyond traditional chemistry sectors.

For quality assurance, technical specifications of 58986-61-1 typically include >98% purity (HPLC), low heavy metal content, and strict control of residual solvents. These parameters are crucial for laboratories requiring ISO-certified reference standards, another frequent search keyword cluster related to this compound.

Emerging research explores the photophysical properties of 3-(Cyclopropylmethoxy)benzaldehyde derivatives for fluorescence probes and photosensitizers. Such studies respond to the increasing demand for "small molecule optical materials" in bioimaging applications, further expanding the compound’s market potential.

In summary, 3-(Cyclopropylmethoxy)benzaldehyde (CAS No. 58986-61-1) represents a multifaceted chemical entity with broad applicability across life sciences, materials engineering, and sustainable technology. Its alignment with contemporary research priorities ensures continued scientific and commercial interest in this structurally intriguing molecule.

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• 153200-64-7(3-(Cyclopropylmethoxy)-4-methoxybenzaldehyde)
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