• 1. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 2. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 3. EWOD-driven droplet microfluidic device integrated with optoelectronic tweezers as an automated platform for cellular isolation and analysis?
  Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
• 4. Excitable dynamics in the bromate–sulfite–ferrocyanide reaction
  J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
• 5. Evidence of rutile-to-anatase photo-induced electron transfer in mixed-phase TiO2 by solid-state NMR spectroscopy?
  Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Aralkylamines
• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Aralkylamines

Introduction to N*1*-Furan-2-ylmethyl-N*1*-isopropyl-ethane-1,2-diamine (CAS No. 1181600-76-9)

N*1*-Furan-2-ylmethyl-N*1*-isopropyl-ethane-1,2-diamine is a significant compound in the realm of chemical and pharmaceutical research, characterized by its unique structural and functional properties. This compound, identified by the CAS number 1181600-76-9, has garnered attention due to its potential applications in various biochemical and medicinal contexts. The molecular structure of this diamine derivative incorporates both furan and isopropyl groups, which contribute to its distinctive chemical behavior and reactivity.

The N*1*-Furan-2-ylmethyl moiety in the compound's name is particularly noteworthy, as it introduces a heterocyclic aromatic ring into the molecular framework. This furan ring is known for its ability to participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. Such properties make it a valuable component in the synthesis of complex molecules and in the development of novel catalysts. The N*1*-isopropyl group further enhances the compound's versatility by providing a steric hindrance that can influence reaction pathways and product selectivity.

In recent years, there has been growing interest in exploring the applications of N*1*-Furan-2-ylmethyl-N*1*-isopropyl-ethane-1,2-diamine in pharmaceutical research. Its unique structural features have led researchers to investigate its potential role as an intermediate in the synthesis of bioactive molecules. For instance, studies have shown that this compound can serve as a precursor for the development of new antibiotics and antiviral agents. The presence of both nitrogen and oxygen atoms in its structure allows for diverse interactions with biological targets, making it a promising candidate for drug discovery.

Moreover, the ethane-1,2-diamine backbone of this compound provides a flexible scaffold that can be modified to tailor specific biological activities. This flexibility has been exploited in the design of novel ligands for metal-based therapeutics. Recent research has highlighted the use of such diamines in the development of metallo-drugs, which have shown efficacy in treating various diseases, including cancer and infectious disorders. The ability of N*1*-Furan-2-ylmethyl-N*1*-isopropyl-ethane-1,2-diamine to coordinate with transition metals has opened up new avenues for therapeutic intervention.

The compound's potential also extends to its role in catalysis. The combination of furan and isopropyl groups creates a molecule that can act as a ligand in transition metal-catalyzed reactions. These reactions are crucial in organic synthesis, where they facilitate the formation of carbon-carbon bonds essential for constructing complex molecules. Researchers have been particularly interested in using this compound as a ligand for palladium and copper catalysts, which are widely employed in pharmaceutical manufacturing due to their high efficiency and selectivity.

From an industrial perspective, N*1*-Furan-2-ylmethyl-N*1*-isopropyl-ethane-1,2-diamine represents a valuable building block for synthesizing more complex chemicals. Its synthesis involves well-established organic reactions that can be scaled up for industrial production. The compound's stability under various conditions makes it suitable for long-term storage and transport, ensuring its availability for research and commercial applications.

The growing body of research on this compound underscores its significance in modern chemistry and pharmaceutical science. As scientists continue to uncover new applications for N*1*-Furan-2-ylmethyl-N*1*-isopropyl-ethane-1,2-diamine, its importance is likely to increase further. The intersection of its unique structural features with cutting-edge research methodologies promises to yield innovative solutions to some of the most pressing challenges in medicine and materials science.

• 741290-33-5(1,2-Ethanediamine,N1-(2-furanylmethyl)-N1-methyl-)
• 1185304-05-5(1-(2-Furylmethyl)piperazine Dihydrochloride)
• 873433-11-5(1-(5-methyl-2-furyl)methylpiperazine)
• 626216-39-5(N'-(2-furylmethyl)-N,N-dimethylethane-1,2-diamine)
• 5700-55-0(1,2-Ethanediamine, N,N'-bis(2-furanylmethyl)-)
• 61695-02-1(1,2-Ethanediamine, N-ethyl-N-(2-furanylmethyl)-)
• 59037-70-6(1-(2-Furylmethyl)piperazine)
• 626216-42-0(2-(dimethylamino)ethyl(5-methylfuran-2-yl)methylamine)
• 415925-67-6(Piperazine,1-ethyl-4-[(5-methyl-2-furanyl)methyl]-)
• 391277-44-4(1,2-Ethanediamine, N,N-bis(2-aminoethyl)-N'-(2-furanylmethyl)-)