• 1. Dissociation of large gaseous serine clusters produces abundant protonated serine octamer
  Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
• 2. Embedding cyclic nitrone in mesoporous silica particles for EPR spin trapping of superoxide and other radicals?
  Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
• 3. Fe/Fe3C@C nanoparticles encapsulated in N-doped graphene–CNTs framework as an efficient bifunctional oxygen electrocatalyst for robust rechargeable Zn–air batteries?
  Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
• 4. Emerging enantiomeric resolution materials with homochiral nano-fabrications
  Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
• 5. 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

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

Exploring Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate (CAS No. 893737-91-2): A Versatile Compound in Modern Chemistry

In the realm of organic chemistry, Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate (CAS No. 893737-91-2) stands out as a compound of significant interest due to its unique structural features and broad applicability. This ester derivative, characterized by a formyl group and a hydroxyl group on its aromatic ring, serves as a pivotal intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty materials. Its molecular architecture, combining both electron-donating and electron-withdrawing substituents, makes it a valuable building block for designing complex molecules with tailored properties.

The growing demand for fine chemicals and high-performance materials has propelled research into compounds like Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate. Recent trends in green chemistry and sustainable synthesis have further highlighted its potential, as researchers explore eco-friendly catalytic methods to produce such intermediates. Questions like "How is Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate synthesized?" or "What are its applications in drug discovery?" are frequently searched, reflecting its relevance in both academic and industrial settings.

One of the most intriguing aspects of Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate is its role in medicinal chemistry. The presence of a hydroxyphenyl moiety allows for facile derivatization, enabling the creation of libraries of compounds for biological screening. This aligns with the current focus on targeted drug design and personalized medicine, where precise molecular modifications are critical. Additionally, its formyl group offers a reactive handle for further functionalization, making it a versatile scaffold for constructing heterocycles and other pharmacophores.

Beyond pharmaceuticals, Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate finds utility in the development of advanced materials. Its aromatic system and functional groups make it a candidate for designing organic semiconductors, photocatalysts, and polymeric coatings. With the rise of renewable energy technologies, researchers are investigating its potential in organic photovoltaics (OPVs) and light-emitting diodes (LEDs), where its electronic properties can be finely tuned.

From a synthetic perspective, the compound's CAS No. 893737-91-2 is often referenced in patents and journals detailing innovative routes to its production. Optimizing its synthesis to reduce waste and improve yield is a hot topic, particularly in the context of circular economy principles. Searches for "scalable synthesis of Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate" or "its spectroscopic characterization" underscore the practical challenges and solutions in its manufacturing.

In conclusion, Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate (CAS No. 893737-91-2) exemplifies the intersection of fundamental chemistry and cutting-edge applications. Its multifaceted utility in drug development, material science, and sustainable chemistry ensures its continued prominence in research and industry. As scientific inquiry evolves, this compound will likely remain a cornerstone for innovation, addressing global challenges in health, energy, and environmental sustainability.

• 1261905-41-2(2-hydroxy-4-(4-methoxycarbonylphenyl)benzoic Acid)
• 1261944-42-6(Methyl 3-(4-formyl-3-hydroxyphenyl)benzoate)
• 4906-69-8([1,1'-Biphenyl]-3-carboxylicacid, 2-hydroxy-, methyl ester)
• 117369-94-5(Methyl 2-hydroxy-4-phenylbenzoate)
• 1258625-58-9(2-Formyl-6-(3-methoxycarbonylphenyl)phenol)
• 40501-40-4(2-(4-Methoxycarbonylphenyl)phenol)
• 1261977-54-1(2-hydroxy-4-(3-methoxycarbonylphenyl)benzoic Acid)
• 1261944-50-6(Methyl 4-(4-formyl-3-hydroxyphenyl)benzoate)
• 1258618-95-9(Methyl 4-(3-formyl-2-hydroxyphenyl)benzoate)
• 92254-28-9(2-(3-Methoxycarbonylphenyl)phenol)