• 1. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 2. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
• 3. Dissociation of aryl sulfonyl phthalimide radical anions: relevance to the biological activity of arylsulfonyl amides?
  Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
• 4. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
• 5. Excimer and exciplex formation in a pair of bright phosphorescent isomers constructed from Cu3(pyrazolate)3 and Cu3I3 coordination luminophores?
  Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459

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

4,4-Dinitrodiphenic Acid (CAS No. 20246-81-5): Properties, Applications, and Market Insights

4,4-Dinitrodiphenic Acid (CAS No. 20246-81-5) is a specialized organic compound with significant applications in advanced material synthesis and chemical research. This yellow crystalline solid, known for its unique molecular structure, has garnered attention in both academic and industrial settings due to its versatile reactivity and potential in high-performance applications.

The chemical structure of 4,4-Dinitrodiphenic Acid features two nitro groups (-NO₂) attached to a biphenyl backbone, contributing to its distinctive electronic properties. Researchers have explored its use as a building block for functional materials, particularly in the development of advanced polymers and coordination complexes. Its thermal stability and electron-withdrawing characteristics make it valuable for designing materials with specific optical or electronic properties.

Recent studies highlight the potential of 4,4-Dinitrodiphenic Acid derivatives in organic electronics, a rapidly growing field addressing the demand for flexible and sustainable electronic components. The compound's ability to form stable complexes with various metals has opened new possibilities in catalysis research and materials science, aligning with current trends in green chemistry and sustainable technology development.

In pharmaceutical research, while not directly used as an active ingredient, 4,4-Dinitrodiphenic Acid serves as an important intermediate for synthesizing more complex molecules. Its structural features make it valuable for creating molecular scaffolds in drug discovery programs, particularly in the development of targeted therapies and diagnostic agents.

The analytical characterization of 4,4-Dinitrodiphenic Acid typically involves techniques such as HPLC, mass spectrometry, and X-ray crystallography. These methods help researchers understand its purity, stability, and molecular interactions - crucial information for applications requiring precise material properties. Recent advancements in analytical instrumentation have improved the ability to study this compound's behavior under various conditions.

From an industrial perspective, the production of 4,4-Dinitrodiphenic Acid requires specialized synthesis routes that balance yield, purity, and environmental considerations. Manufacturers are increasingly adopting green chemistry principles in its production, responding to the growing demand for sustainable chemical processes. The compound's market has seen steady growth, particularly in regions with strong advanced materials and pharmaceutical research sectors.

Storage and handling of 4,4-Dinitrodiphenic Acid require standard laboratory precautions for organic compounds. While not classified as hazardous under normal conditions, proper chemical safety protocols should always be followed. The compound is typically stable at room temperature when stored in appropriate containers protected from moisture and direct sunlight.

Research trends indicate growing interest in modifying the 4,4-Dinitrodiphenic Acid structure to create new derivatives with enhanced properties. Scientists are exploring its potential in energy storage materials, molecular sensors, and specialty coatings. These developments align with current technological needs in renewable energy and smart materials.

For researchers working with 4,4-Dinitrodiphenic Acid, understanding its solubility characteristics and reactivity patterns is essential. The compound exhibits moderate solubility in polar organic solvents but limited solubility in water, which influences its applications in various chemical processes. Recent publications have focused on optimizing reaction conditions to maximize its utility in synthetic chemistry.

The future outlook for 4,4-Dinitrodiphenic Acid appears promising, with potential expansions into emerging technology sectors. As material science continues to advance, the demand for specialized organic building blocks like this compound is expected to grow, particularly in applications requiring precise molecular control and tailored material properties.

• 92159-34-7(2-(2-carboxy-5-nitrophenyl)-4-nitrobenzoic Acid)
• 62199-60-4(4-Nitro-2'-carboxybiphenyl)
• 37174-74-6(3'-Nitro-[1,1'-biphenyl]-2-carboxylic acid)
• 1261952-79-7(2'-Methyl-5-nitro-1,1'-biphenyl-3-carboxylic Acid)
• 1261977-06-3(2-(3-methylphenyl)-4-nitrobenzoic Acid)
• 1261980-20-4(2-(2,3-dimethylphenyl)-4-nitrobenzoic Acid)
• 1261943-66-1(2-(3-aminophenyl)-4-nitrobenzoic Acid)
• 1261923-66-3(2-[3-(hydroxymethyl)phenyl]-4-nitrobenzoic Acid)
• 1261953-43-8(2-(4-methylphenyl)-4-nitrobenzoic Acid)
• 1261984-13-7(2-(3-formylphenyl)-4-nitrobenzoic Acid)