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• 2. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
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• 5. 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 Organoheterocyclic compounds Heteroaromatic compounds Heteroaromatic compounds
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Heteroaromatic compounds
• Solvents and Organic Chemicals Organic Compounds Heterocyclic Compounds
• Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides

Exploring the Unique Properties and Applications of 2-(Furfurylthio)ethylamine (CAS No. 36415-21-1)

2-(Furfurylthio)ethylamine (CAS No. 36415-21-1) is a fascinating sulfur-containing amine derivative that has garnered significant attention in both academic and industrial research. This compound, characterized by its furfurylthio and ethylamine functional groups, exhibits unique chemical properties that make it valuable in various applications, from flavor and fragrance chemistry to advanced material synthesis. In this comprehensive overview, we delve into its molecular structure, synthesis pathways, and emerging uses in cutting-edge fields like green chemistry and biodegradable materials.

The molecular formula of 2-(Furfurylthio)ethylamine is C7H11NOS, with a molar mass of 157.23 g/mol. Its structure combines a furan ring linked to a thioether group, followed by an ethylamine chain. This arrangement imparts distinctive reactivity, particularly in nucleophilic substitution reactions and as a building block for heterocyclic compounds. Researchers have explored its potential as a precursor for flavor enhancers, given its ability to contribute roasted, nutty, or meat-like aromas—a property highly sought after in the food industry.

Recent studies highlight the role of 2-(Furfurylthio)ethylamine in sustainable chemistry initiatives. As industries shift toward eco-friendly alternatives, this compound's derivates show promise in bio-based polymers and non-toxic catalysts. Its sulfur moiety enables chelation with metal ions, making it relevant in wastewater treatment technologies where heavy metal removal is critical. Additionally, its compatibility with enzymatic reactions aligns with the growing demand for biocatalysis in pharmaceutical intermediates.

From a commercial perspective, the global market for specialty amines like 2-(Furfurylthio)ethylamine is expanding, driven by trends in personal care products and functional additives. Its mild odor profile and stability under physiological conditions have led to investigations in cosmetic formulations, particularly in hair care products where sulfur-containing compounds improve keratin integrity. Furthermore, its application in agrochemicals as a synergist for pesticides reflects the compound's versatility.

Safety and handling of 2-(Furfurylthio)ethylamine adhere to standard laboratory protocols. While not classified as hazardous under major regulatory frameworks, proper ventilation and personal protective equipment (PPE) are recommended during handling. Storage in amber glass containers under inert atmosphere enhances its shelf life, preventing oxidative degradation of the thioether group—a common query among first-time users searching for "how to store sulfur-containing amines."

Innovations in synthesis methods have reduced production costs, making 2-(Furfurylthio)ethylamine more accessible. Microwave-assisted reactions and flow chemistry techniques now achieve higher yields compared to traditional batch processes—a topic frequently discussed in "amine synthesis optimization" forums. These advancements align with the principles of circular economy, as byproducts can be repurposed into value-added chemicals.

Looking ahead, 2-(Furfurylthio)ethylamine holds untapped potential in electronic materials. Preliminary research suggests its utility in modifying conductive polymers for flexible electronics, answering the rising popularity of searches like "organic semiconductors from biomass." As interdisciplinary collaborations grow, this compound may bridge gaps between renewable resources and high-tech applications, solidifying its position in next-generation smart materials.

• 40228-18-0(Furan,[(methylthio)methyl]-)
• 13678-67-6(2-(Furan-2-ylmethylsulfanylmethyl)furan)
• 13679-60-2(Furan,2-methyl-5-[(methylthio)methyl]-)
• 114914-08-8(Furan,2-[[(3-chloropropyl)thio]methyl]-)
• 86251-28-7(2-((Furan-2-ylmethyl)thio)acetamide)
• 66356-54-5(5-(2-Aminoethyl)thiomethyl-N-methyl-2-furanmethanamine)
• 60116-24-7(Ethanamine, 2-[(2-furanylmethyl)thio]-, hydrochloride)
• 1438-91-1(Methyl Furfuryl Sulfide)
• 1883-78-9(Furfuryl Isopropyl Sulfide)
• 2024-70-6(Furan,2-[(ethylthio)methyl]-)