• 1. Synthesis of β-carboline–benzimidazole conjugates using lanthanum nitrate as a catalyst and their biological evaluation
  Ahmed Kamal,M. P. Narasimha Rao,P. Swapna,Vunnam Srinivasulu,Chandrakant Bagul,Anver Basha Shaik,Kishore Mullagiri,Jeshma Kovvuri,Vangala Santhosh Reddy,K. Vidyasagar,Narayana Nagesh Org. Biomol. Chem. 2014 12 2370
• 2. A facile atom economic one pot multicomponent synthesis of bioactive spiro-indenoquinoxaline pyrrolizines as potent antioxidants and anti-cancer agents
  Kailasam Saravana Mani,Werner Kaminsky,Subramaniam Parameswaran Rajendran New J. Chem. 2018 42 301
• 3. A metal–organic framework based multifunctional catalytic platform for organic transformation and environmental remediation
  Harpreet Kaur,M. Venkateswarulu,Suneel Kumar,Venkata Krishnan,Rik Rani Koner Dalton Trans. 2018 47 1488
• 4. Synthesis, DNA interaction and anticancer activity of 2-anthryl substituted benzimidazole derivatives
  Vyankat A. Sontakke,Anup N. Kate,Sougata Ghosh,Piyush More,Rajesh Gonnade,Navanath M. Kumbhar,Anupa A. Kumbhar,Balu A. Chopade,Vaishali S. Shinde New J. Chem. 2015 39 4882
• 5. Surfactant-induced disaggregation of a quinoxaline AIEgen scaffold: aggregation aptitude in the solid and solution states
  Sagnik De,Gopal Das Soft Matter 2023 19 6116

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

3,4-Diaminobenzophenone: A Comprehensive Overview

3,4-Diaminobenzophenone, also known by its CAS number 39070-63-8, is a significant compound in the field of organic chemistry. This compound is a derivative of benzophenone, featuring two amino groups (-NH?) attached to the benzene ring at the 3 and 4 positions. The molecular structure of 3,4-Diaminobenzophenone makes it highly versatile and valuable in various applications across different industries.

The synthesis of 3,4-Diaminobenzophenone involves several methods, including the reduction of nitro groups or the direct coupling of amines with benzophenone derivatives. Recent advancements in catalytic systems have enabled more efficient and selective syntheses, reducing production costs and environmental impact. These methods are particularly relevant in the context of green chemistry, where minimizing waste and maximizing yields are critical.

3,4-Diaminobenzophenone has found extensive use in the field of materials science. Its ability to form stable coordination complexes with transition metals has made it a valuable precursor for synthesizing metal-organic frameworks (MOFs) and other porous materials. MOFs are widely used in gas storage, catalysis, and sensing applications due to their high surface area and tunable properties.

In the pharmaceutical industry, 3,4-Diaminobenzophenone serves as an intermediate in the synthesis of various bioactive compounds. Recent studies have highlighted its role in the development of potential anticancer agents. For instance, researchers have explored its ability to inhibit specific enzymes involved in tumor growth and metastasis. These findings underscore its potential as a lead compound for drug discovery.

The electronic properties of 3,4-Diaminobenzophenone make it an attractive candidate for applications in organic electronics. Its conjugated system allows for efficient charge transport, which is essential for devices such as organic light-emitting diodes (OLEDs) and field-effect transistors (FETs). Recent breakthroughs in molecular design have further enhanced its performance in these devices, paving the way for next-generation electronic materials.

3,4-Diaminobenzophenone also plays a crucial role in chemical synthesis as a building block for more complex molecules. Its amino groups provide sites for further functionalization, enabling the creation of diverse structures with tailored properties. This versatility has made it a cornerstone in synthetic chemistry, particularly in the construction of heterocyclic compounds and polymeric materials.

The environmental impact of 3,4-Diaminobenzophenone has been a topic of recent research interest. Studies have focused on its biodegradation pathways and potential toxicity to aquatic organisms. Understanding these aspects is essential for ensuring sustainable practices in its production and application.

In conclusion, 3,4-Diaminobenzophenone, with its CAS number 39070-63-8, stands out as a multifaceted compound with applications spanning materials science, pharmaceuticals, electronics, and synthetic chemistry. Ongoing research continues to uncover new possibilities for this compound, solidifying its importance in both academic and industrial settings.

• 611-79-0(3-(3-aminobenzoyl)aniline)
• 2835-78-1(3-Aminobenzophenone)
• 62261-45-4(Methanone, (3-amino-5-methylphenyl)phenyl-)
• 62261-36-3(Methanone, (3-aminophenyl)(4-methylphenyl)-)
• 57070-71-0(4-Benzoylbenzene-1,2-diamine Hydrochloride)
• 62261-60-3(Methanone, (3-aminophenyl)(4-ethylphenyl)-)
• 33848-56-5(Acetophenone, 3,4-diamino-, conjugate diacid (8CI))
• 21304-39-2(1-(3,4-Diaminophenyl)ethanone)
• 51458-66-3(Methanone,(3-aminophenyl)(4-aminophenyl)-)
• 62261-46-5(Methanone, (3-aminophenyl)(3-methylphenyl)-)