26306-01-4 Usage
Uses
Used in the Plastics Industry:
[(6-Iodohexyl)oxy]trimethylsilane is utilized as a silane coupling agent, enhancing the adhesion and compatibility of various materials in the production of plastics. Its strong bonding capabilities improve the overall quality and durability of the final plastic products.
Used in the Adhesives Industry:
In the adhesives sector, [(6-Iodohexyl)oxy]trimethylsilane serves as a crucial component in the formulation of high-performance adhesives. It ensures better bonding between different substrates, leading to more reliable and long-lasting adhesive products.
Used in the Coatings Industry:
[(6-Iodohexyl)oxy]trimethylsilane is also employed in the development of coatings, where it contributes to the improved adhesion and durability of the coating on various surfaces, including metals, plastics, and other materials.
Used in Organic Synthesis:
[(6-Iodohexyl)oxy]trimethylsilane acts as a reagent in organic synthesis, facilitating the creation of new compounds and materials with specific properties and applications.
Used as a Hydrophobizing Agent for Mineral Surfaces:
This chemical is used to make mineral surfaces more hydrophobic, which can be beneficial in various applications, such as improving the water repellency of materials or enhancing the performance of products in wet conditions.
Used in the Pharmaceutical Industry:
[(6-Iodohexyl)oxy]trimethylsilane is also utilized as an intermediate in the development of pharmaceuticals, playing a role in the synthesis of various drugs and medications.
Used in the Agrochemicals Industry:
Similarly, in the agrochemicals sector, the compound is used as an intermediate for the synthesis of different agrochemical products, contributing to the development of more effective and targeted solutions for agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 26306-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,3,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26306-01:
(7*2)+(6*6)+(5*3)+(4*0)+(3*6)+(2*0)+(1*1)=84
84 % 10 = 4
So 26306-01-4 is a valid CAS Registry Number.
26306-01-4Relevant academic research and scientific papers
Cyclic ethers as educts for the synthesis of lepidoptra pheromones
Poleschner,Heydenreich,Martin
, p. 1231 - 1235 (2007/10/02)
ω-Iodo(trialkylsiloxy)alkanes 2 prepared by ring opening of cyclic ethers with iodotrimethylsilane, are useful starting materials for the synthesis of pheromone components. Reaction with triphenylphosphine to give the corresponding Wittig reagent and subsequent coupling with lithium (Z)-dihex-1-enylcuprate gives (Z)-alken-1-ols 5 and 7, after deprotection, in good yields. The direct coupling of 2 with alkynes failed because of competition reactions, however, the more stable ω-iodo-1-(tert-butyldimethylsiloxy)alkanes were able to undergo C,C-coupling with alkynes. The thus formed 1-(tert-butyldimethylsiloxy)-5-decyne (13c) was hydrogenated and deprotected to give (E)-5-decen-1-ol (15c).
Studies in the Biosynthesis of -Gingerol, Pungent Principle of Ginger (Zingiber officinale)
Denniff, Phillip,Whiting, Donald A.
, p. 2637 - 2644 (2007/10/02)
The biosynthesis of -gingerol has been investigated by the administration of labelled precursors to whole Zingiber officinale plants and to rhizome sections.The results show that phenylalanine is elaborated to ferulic acid which then condenses, in an unusual version of the 'biological Claisen' reaction, with malonate and hexanoate to yield -dehydrogingerdione (11).Hexanoate is incorporated intact as shown by the location of label and the constancy of isotope ratios.Dihydroferulate is accepted, but loss of tritium shows it to be first dehydrogenated.Dione (11) is reduced in two steps to -gingerol; in the preferred path, C=O reduction precedes C=C reduction, with (12) as intermediate, although dione (13) is also converted.
