• 1. Emerging enantiomeric resolution materials with homochiral nano-fabrications
  Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
• 2. Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides?
  Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
• 3. Evolution study of photo-synthesized gold nanoparticles by spectral deconvolution model: a quantitative approach
  Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
• 4. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 5. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Phenylpropanes

Compound CAS No 7681-79-0: 2-Ethyl(methyl)amino-1-phenylpropan-1-ol

The compound with CAS No 7681-79-0, known as 2-Ethyl(methyl)amino-1-phenylpropan-1-ol, is a fascinating organic molecule that has garnered significant attention in the fields of chemistry and pharmacology. This compound is characterized by its unique structure, which includes a phenyl group, an amino alcohol functional group, and a branched alkyl chain. The phenyl group contributes to its aromatic properties, while the amino alcohol functionality imparts hydrophilic characteristics, making it versatile for various applications.

Recent studies have highlighted the potential of 2-Ethyl(methyl)amino-1-phenylpropan-1-ol in drug discovery and development. Researchers have explored its role as a precursor in the synthesis of bioactive molecules, particularly in the development of neuroprotective agents and anti-inflammatory drugs. The compound's ability to interact with biological systems through its amino and hydroxyl groups makes it an attractive candidate for medicinal chemistry research.

In terms of synthesis, 2-Ethyl(methyl)amino-1-phenylpropan-1-ol can be prepared through a variety of methods, including nucleophilic substitution reactions and catalytic hydrogenation. One notable approach involves the reaction of an appropriate phenolic derivative with an amine-containing reagent under specific conditions. This method not only ensures high yields but also allows for fine-tuning of the product's properties by modifying the reaction parameters.

The structural versatility of this compound has also led to its use in materials science. For instance, it has been employed as a building block in the synthesis of advanced polymers and surfactants. Its ability to form stable emulsions and its compatibility with various solvents make it valuable in industries such as coatings and personal care products.

From an environmental perspective, the biodegradability and toxicity profile of 2-Ethyl(methyl)amino-1-phenylpropan-1-ol have been thoroughly investigated. Studies indicate that it exhibits low toxicity to aquatic organisms under standard test conditions, which aligns with its potential use in eco-friendly applications. However, further research is needed to fully understand its long-term environmental impact.

Looking ahead, the integration of computational chemistry techniques, such as molecular docking and quantum mechanics simulations, promises to deepen our understanding of this compound's interactions at the molecular level. Such insights could pave the way for innovative applications in drug delivery systems and enzyme inhibition studies.

In conclusion, 2-Ethyl(methyl)amino-1-phencylpropan-1 ol (CAS No 7681 -79 -0) stands out as a multifaceted compound with promising prospects across diverse scientific domains. Its unique chemical properties, coupled with ongoing advancements in synthetic methodologies and computational tools, ensure that this molecule will continue to be a subject of interest for researchers worldwide.

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