• 1. A heterogeneous Ru/CeO2 catalyst effective for transfer-allylation from homoallyl alcohols to aldehydes
  Hiroki Miura,Kenji Wada,Saburo Hosokawa,Masahiro Sai,Teruyuki Kondo,Masashi Inoue catalyst effective for transfer-allylation from homoallyl alcohols to aldehydes. Hiroki Miura Kenji Wada Saburo Hosokawa Masahiro Sai Teruyuki Kondo Masashi Inoue Chem. Commun. 2009 4112
• 2. 934. Reactions of organic peroxides. Part VIII. 1 : 3 : 3-Trimethylindan-1-yl hydroperoxide and its conversion into 2 : 4 : 4-trimethylchroman derivatives
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Indenes and isoindenes Indenes and isoindenes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Indenes and isoindenes

Comprehensive Guide to 1,1,3-Trimethyl-1H-indene (CAS No. 2177-45-9): Properties, Applications, and Market Insights

1,1,3-Trimethyl-1H-indene (CAS No. 2177-45-9) is a specialized organic compound belonging to the indene family. This compound has garnered significant attention in recent years due to its unique chemical structure and versatile applications in various industries. With the increasing demand for high-performance materials and specialty chemicals, 1,1,3-Trimethyl-1H-indene has become a subject of interest for researchers and industrial professionals alike.

The molecular formula of 1,1,3-Trimethyl-1H-indene is C12H14, and it features a fused benzene and cyclopentene ring system with three methyl substituents. This structural configuration imparts distinct chemical and physical properties that make it valuable for numerous applications. Recent studies have highlighted its potential in the development of advanced polymers, fragrances, and pharmaceutical intermediates, aligning with current trends in sustainable chemistry and green synthesis.

One of the most frequently asked questions about 1,1,3-Trimethyl-1H-indene is its role in polymer chemistry. The compound serves as a key monomer or intermediate in the synthesis of high-performance resins and coatings. Its ability to enhance thermal stability and mechanical strength in polymers makes it particularly relevant in industries such as automotive, aerospace, and electronics, where durability and performance are critical.

Another trending topic related to 1,1,3-Trimethyl-1H-indene is its application in fragrance formulations. The compound's aromatic characteristics contribute to the creation of long-lasting and complex scent profiles, making it a popular choice in the perfumery and cosmetics industries. As consumers increasingly seek unique and sustainable fragrance options, the demand for innovative ingredients like 1,1,3-Trimethyl-1H-indene continues to rise.

From a market perspective, the global demand for 1,1,3-Trimethyl-1H-indene is expected to grow steadily, driven by advancements in material science and the expanding personal care sector. Industry reports indicate that Asia-Pacific regions, particularly China and India, are emerging as key players in the production and consumption of this compound, reflecting broader trends in chemical manufacturing and innovation.

Researchers are also exploring the potential of 1,1,3-Trimethyl-1H-indene in pharmaceutical applications. Preliminary studies suggest that its structural features could be leveraged to develop novel drug candidates, especially in areas such as anti-inflammatory and antimicrobial therapies. This aligns with the growing focus on drug discovery and the need for new chemical entities in the healthcare sector.

In terms of synthesis, modern approaches to producing 1,1,3-Trimethyl-1H-indene emphasize efficiency and environmental sustainability. Catalytic methods and green chemistry principles are being increasingly adopted to minimize waste and reduce energy consumption, addressing the industry's shift toward more sustainable practices. These advancements are particularly relevant given the current emphasis on reducing carbon footprints and adhering to stringent environmental regulations.

For those seeking detailed technical specifications, 1,1,3-Trimethyl-1H-indene typically appears as a colorless to pale yellow liquid with a characteristic aromatic odor. Its boiling point ranges between 220-230°C, and it exhibits moderate solubility in common organic solvents. These properties make it suitable for various formulation and processing requirements in industrial applications.

Safety and handling of 1,1,3-Trimethyl-1H-indene are also critical considerations. While the compound is not classified as hazardous under standard regulations, proper storage conditions—such as keeping it in a cool, dry place away from direct sunlight—are recommended to maintain its stability and shelf life. Material safety data sheets (MSDS) provide comprehensive guidelines for safe handling and disposal, ensuring compliance with workplace safety standards.

Looking ahead, the future of 1,1,3-Trimethyl-1H-indene appears promising, with ongoing research uncovering new applications and improved synthesis methods. As industries continue to prioritize innovation and sustainability, this compound is poised to play a pivotal role in the development of next-generation materials and specialty chemicals. Whether in polymers, fragrances, or pharmaceuticals, 1,1,3-Trimethyl-1H-indene exemplifies the intersection of chemistry and cutting-edge technology.

• 30098-23-8(1H-Indene,3-methyl-1,1-diphenyl-)
• 62291-85-4(1H-Indene, 1-ethenyl-1,3-dimethyl-)
• 14656-06-5(1H-Indene,1,1,3,5-tetramethyl-)
• 2177-48-2(1,3-dimethyl-1H-indene)
• 22360-62-9(1H-Indene, 1-methyl-3-phenyl-)
• 138036-89-2(1H-Indene, 3-(1-methyl-1-phenylethyl)-)
• 77242-77-4(1,1,2,3,4,5,6-Heptamethyl-1H-indene)
• 4467-88-3(1,3-diphenyl-1h-indene)
• 89057-44-3(5,5,10,10-Tetramethyl-5,10-dihydroindeno[2,1-a]indene)
• 4614-01-1(1H-Indene,1,1,3-triphenyl-)