• 1. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
• 2. 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
• 3. Evidence for the intrinsic nature of band-gap states electrochemically observed on atomically flat TiO2(110) surfaces?
  Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
• 4. Excellent energy storage performance in NaNbO3-based relaxor antiferroeic ceramics under a low electric field
  XuxinCheng,XiaomingChen,PengyuanFan
• 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 Nitrobenzenes
• Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides

Comprehensive Guide to 2-Iodo-4-nitroaniline (CAS No. 6293-83-0): Properties, Applications, and Market Insights

2-Iodo-4-nitroaniline (CAS No. 6293-83-0) is a specialized organic compound widely used in pharmaceutical and chemical research. With the growing interest in nitroaniline derivatives and iodo-substituted compounds, this chemical has gained attention for its unique properties and versatile applications. In this article, we explore its molecular structure, synthesis methods, industrial uses, and emerging trends in research.

The molecular formula of 2-Iodo-4-nitroaniline is C6H5IN2O2, featuring an iodine atom at the 2-position and a nitro group at the 4-position of the aniline ring. This structural configuration contributes to its reactivity, making it valuable in organic synthesis and pharmaceutical intermediates. Researchers often search for "2-Iodo-4-nitroaniline solubility" or "synthesis of 2-Iodo-4-nitroaniline," highlighting its importance in laboratory settings.

One of the key applications of 2-Iodo-4-nitroaniline is in the development of dyes and pigments. Due to its nitro and amino functional groups, it serves as a precursor in producing colorants for textiles and industrial coatings. Additionally, its iodine component enhances its utility in cross-coupling reactions, a topic frequently searched in organic chemistry forums.

In pharmaceutical research, 2-Iodo-4-nitroaniline is explored for its potential in drug discovery. Its structural motifs are found in compounds with antimicrobial and anti-inflammatory properties. Recent studies investigate its role in catalysis and material science, aligning with trends in green chemistry and sustainable synthesis.

The market for 2-Iodo-4-nitroaniline is influenced by demand from research laboratories and specialty chemical manufacturers. Suppliers often optimize content around keywords like "buy 2-Iodo-4-nitroaniline" or "6293-83-0 supplier" to meet buyer needs. Regulatory compliance and high-purity standards are critical factors in its commercial distribution.

Handling 2-Iodo-4-nitroaniline requires adherence to laboratory safety protocols. While not classified as hazardous under standard conditions, proper storage away from light and moisture is recommended. Researchers frequently ask about "2-Iodo-4-nitroaniline stability" and "storage conditions for nitroaniline compounds," emphasizing the need for clear guidelines.

Future prospects for 2-Iodo-4-nitroaniline include advancements in catalytic applications and biomedical research. Innovations in iodo-organic chemistry may expand its utility in electronic materials and agrochemicals. As interest grows in functionalized anilines, this compound remains a focal point for scientific and industrial exploration.

For those seeking detailed technical data, resources on "2-Iodo-4-nitroaniline spectroscopic analysis" or "CAS 6293-83-0 MSDS" are widely available. Collaborative efforts between academia and industry continue to uncover new possibilities for this versatile chemical.

• 10394-64-6(3-Iodo-5-nitroaniline)
• 105752-04-3(Benzenamine,4-iodo-3-nitro-)
• 5398-27-6(2,6-Diiodo-4-nitroaniline)
• 102153-71-9(2-Iodo-3-nitronaphthalene)
• 709-49-9(2,4-Dinitroiodobenzene)
• 6276-04-6(1-Iodo-3,5-dinitrobenzene)
• 1608-46-4(Benzene,1,2-diiodo-4-nitro-)
• 5459-50-7(2-Iodo-5-nitroaniline)
• 54292-20-5(Benzenamine, 2-iodo-4,6-dinitro-)
• 57830-60-1(1,3-diiodo-5-nitrobenzene)