• 1. Distinction of trans–cis photoisomers with comparable optical properties in multiple-state photochromic systems – examining a molecule with three azobenzenes via in situ irradiation NMR spectroscopy?
  Jonas Kind,Lukas Kaltschnee,Martin Leyendecker,Christina M. Thiele Chem. Commun., 2016,52, 12506-12509
• 2. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets?
  Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283
• 3. 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
• 4. Ester-directed orthogonal dual C–H activation and ortho aryl C–H alkenylation via distal weak coordination?
  Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
• 5. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147

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

Comprehensive Overview of Stannane, tributyl(4-methylphenyl)- (CAS No. 31614-66-1)

Stannane, tributyl(4-methylphenyl)- (CAS No. 31614-66-1) is an organotin compound widely utilized in industrial and research applications. This chemical, characterized by its tributyltin and 4-methylphenyl functional groups, plays a significant role in catalysis, material science, and organic synthesis. Its unique molecular structure makes it a valuable intermediate in the production of specialized polymers, coatings, and agrochemicals. With increasing interest in sustainable chemistry, researchers are exploring its potential in green synthesis and environmentally friendly processes.

The compound's CAS No. 31614-66-1 is a critical identifier for regulatory compliance and safety documentation. Industries often search for "Stannane, tributyl(4-methylphenyl)- uses" or "31614-66-1 applications" to understand its versatility. Recent studies highlight its role in cross-coupling reactions, a hot topic in pharmaceutical and fine chemical manufacturing. As the demand for efficient catalysts grows, this compound's relevance in palladium-catalyzed reactions and carbon-carbon bond formation has garnered attention.

Environmental and health considerations are paramount when handling Stannane, tributyl(4-methylphenyl)-. Users frequently inquire about "31614-66-1 safety data" or "organotin compound toxicity," reflecting heightened awareness of chemical safety. While not classified as hazardous under standard conditions, proper storage and handling protocols are essential. Innovations in green chemistry aim to reduce the ecological footprint of such compounds, aligning with global sustainability goals.

In the realm of material science, CAS No. 31614-66-1 is investigated for its role in advanced coatings and adhesives. Searches like "tributyl(4-methylphenyl)stannane in polymers" indicate its niche applications. The compound's thermal stability and reactivity make it suitable for high-performance materials, including those used in electronics and automotive industries. Researchers are also examining its potential in nanotechnology, where precise molecular control is crucial.

The synthesis and purification of Stannane, tributyl(4-methylphenyl)- require specialized expertise. Queries such as "how to synthesize 31614-66-1" or "purification methods for organotin compounds" are common among chemists. Advanced techniques like column chromatography and distillation are often employed to achieve high purity. As analytical methods evolve, the compound's characterization using NMR spectroscopy and mass spectrometry has become more precise.

Market trends indicate a steady demand for CAS No. 31614-66-1, driven by its applications in specialty chemicals. Keywords like "buy tributyl(4-methylphenyl)stannane" or "31614-66-1 suppliers" reflect commercial interest. Regulatory frameworks, such as REACH and EPA guidelines, influence its global trade, prompting suppliers to provide comprehensive technical data sheets. The compound's niche applications ensure its continued relevance in both academic and industrial settings.

Future research on Stannane, tributyl(4-methylphenyl)- may focus on optimizing its catalytic efficiency and reducing environmental impact. Searches for "sustainable organotin catalysts" or "31614-66-1 alternatives" underscore this shift. Collaborative efforts between academia and industry are likely to yield innovative applications, further solidifying its position in modern chemistry. As the scientific community prioritizes eco-friendly solutions, this compound's adaptability will be key to its longevity.

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