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• 2. Alumina grafted SBA-15 sustainable bifunctional catalysts for direct cross-coupling of benzylic alcohols to diarylmethanes?
  Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
• 3. An artificial photosynthetic system for photoaccumulation of two electrons on a fused dipyridophenazine (dppz)–pyridoquinolinone ligand?
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• Solvents and Organic Chemicals Organic Compounds Organometallic compounds Organometalloid compounds Organosilicon compounds Alkylsilanes

(6-Chlorohex-1-yn-1-yl)trimethylsilane: A Comprehensive Overview

(6-Chlorohex-1-yn-1-yl)trimethylsilane, also known by its CAS number 113964-33-3, is a unique organosilicon compound that has garnered significant attention in the fields of organic synthesis and materials science. This compound is characterized by its trimethylsilyl group attached to a chlorohexynyl chain, which imparts it with distinctive chemical properties and reactivity. In recent years, advancements in synthetic methodologies and its applications in various industries have made it a subject of extensive research.

The molecular structure of (6-Chlorohex-1-yn-1-yl)trimethylsilane consists of a trimethylsilyl group (-SiMe?) linked to a six-carbon chain containing a terminal alkyne group (-C≡CH) and a chlorine atom at the sixth position. This structure endows the compound with both nucleophilic and electrophilic reactivity, making it versatile in organic transformations. The presence of the alkyne group allows for various functionalization reactions, such as hydroamination, hydroxylation, and cycloaddition processes, which are critical in modern organic synthesis.

Recent studies have highlighted the potential of (6-Chlorohex-1-yn-1-yl)trimethylsilane as a valuable precursor in the synthesis of complex organic molecules. For instance, researchers have employed this compound in the construction of biologically active compounds, such as peptide mimetics and macrocyclic structures. Its ability to undergo controlled alkyne chemistry has been exploited to design novel drug delivery systems and bioconjugates, showcasing its relevance in medicinal chemistry.

In addition to its role in organic synthesis, (6-Chlorohex-1-yn-1-yli)trimethylsilane has found applications in materials science, particularly in the development of low-dimensional materials and functional polymers. The compound's reactivity enables the formation of covalent networks with tailored properties, which are essential for applications in electronics, sensors, and advanced composites.

The synthesis of (6-Chlorohexaenyl)trimethylsilane typically involves multi-step processes that require precise control over reaction conditions to ensure high yields and product purity. Recent advancements in catalytic methods and transition-metal-mediated reactions have improved the efficiency of these syntheses, making them more accessible for large-scale production.

From a toxicological perspective, understanding the safety profile of (6-Chlorohexaenyl)trimethylsilane is crucial for its industrial applications. Studies have shown that exposure to this compound may pose certain health risks; however, proper handling protocols and protective measures can mitigate these hazards effectively.

In conclusion, (6-Chlorohexaenyl)trimethylsilane stands as a pivotal compound in contemporary chemical research due to its unique properties and diverse applications. As ongoing research continues to uncover new avenues for its utilization, this compound is poised to play an increasingly significant role in advancing both academic and industrial endeavors.

• 88736-97-4(Silane, 1,8-nonadiyne-1,9-diylbis[trimethyl-)
• 63873-32-5(Silane,1,1'-(1,7-octadiyne-1,8-diyl)bis[1,1,1-trimethyl-)
• 15719-56-9(Silane,1-heptyn-1-yltrimethyl-)
• 15719-55-8(Silane, trimethyl-1-octynyl-)
• 54559-17-0(Silane, 1-decynyltrimethyl-)
• 174125-30-5(Silane,(5-chloro-1-pentyn-1-yl)triethyl-)
• 77113-48-5(Silane,(5-chloro-1-pentyn-1-yl)trimethyl-)
• 3844-94-8(1-Trimethylsilyl-1-hexyne)
• 88736-99-6(Silane, 1,17-octadecadiyne-1,18-diylbis[trimethyl-)
• 88736-98-5(Silane, 1,9-decadiyne-1,10-diylbis[trimethyl-)