• 1. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
• 2. 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
• 3. Dissociative dynamics of O2 on Ag(110)?
  Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
• 4. Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices
  Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
• 5. Emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) of styrene: poly(dimethylaminoethyl methacrylate) macro-TERP agent?
  Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792

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

Exploring the Potential of 2-Propanone, 1-(4-Hydroxy-3-Methylphenyl)-: A Comprehensive Overview

The compound 2-Propanone, 1-(4-hydroxy-3-methylphenyl)-, also known by its CAS Registry Number 88659-81-8, has garnered significant attention in the field of biopharmaceuticals due to its unique chemical structure and potential applications. This compound belongs to a class of organic molecules that combine ketone functionality with aromatic ring substituents, making it a subject of interest for researchers exploring pharmacological agents and bioactive compounds.

Recent studies have highlighted the importance of understanding the biological activity of such compounds in drug discovery. The presence of the 4-hydroxy-3-methylphenyl group attached to the ketone moiety introduces a degree of complexity that could potentially be leveraged for designing targeted therapies. This structural feature not only influences the compound's solubility and stability but also plays a critical role in determining its interactions with biological systems.

One of the key areas of research involving 2-Propanone, 1-(4-hydroxy-3-methylphenyl)- is its potential as a bioisostere in medicinal chemistry. By modifying the substituents on the aromatic ring, scientists can explore how these changes affect the compound's pharmacokinetics and bioavailability. For instance, the hydroxyl group at position 4 introduces hydrogen bonding capabilities, which could enhance the molecule's ability to interact with biological targets.

Another important aspect of this compound is its synthetic accessibility. The ketone functionality makes it a suitable candidate for various coupling reactions and post-synthesis modifications. This ease of manipulation is particularly advantageous in drug development, where the need for rapid prototyping and optimization is critical. Additionally, the presence of the methyl group at position 3 adds to the compound's structural diversity, offering potential for tailored applications.

Recent advancements in computational chemistry have further enhanced our understanding of 2-Propanone, 1-(4-hydroxy-3-methylphenyl)-. Through molecular modeling and docking studies, researchers have gained insights into how the compound's electronic properties and spatial arrangement could influence its binding affinity to various receptors and enzymes. These findings are instrumental in guiding the design of more effective drugs with reduced off-target effects.

Moreover, the compound's antimicrobial properties have been explored in several recent studies. The combination of a ketone group and an aromatic ring with hydroxyl substituents creates a unique environment that may disrupt bacterial cell membranes or inhibit key enzymes involved in pathogenesis. This makes it a promising candidate for developing new generations of antibiotics, which are increasingly needed due to the rise of antibiotic resistance.

In conclusion, 2-Propanone, 1-(4-hydroxy-3-methylphenyl)- (CAS NO 88659-81-8) represents a fascinating compound with diverse applications in the biopharmaceutical industry. Its unique structure, coupled with its potential for modification and optimization, positions it as a valuable tool in drug discovery and development. As research continues to uncover new insights into its biological activity and chemical properties, this compound is likely to play an even more significant role in addressing unmet medical needs.

• 770-39-8(4-Hydroxyphenylacetone)
• 13100-05-5(1-(2-Hydroxyphenyl)propan-2-one)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)