26306-01-4 Usage
General Description
[(6-Iodohexyl)oxy]trimethylsilane is a chemical compound with the molecular formula C9H21IO2Si. It is a colorless or light yellow liquid with a pungent odor. This chemical is primarily used as a silane coupling agent in the production of plastics, adhesives, and coatings. It can also be used as a reagent in organic synthesis and as a hydrophobizing agent for mineral surfaces. Furthermore, it is utilized as an intermediate for pharmaceuticals and agrochemicals. [(6-Iodohexyl)oxy]trimethylsilane is known for its ability to form strong bonds between organic and inorganic materials, making it a valuable tool in various industrial processes. However, it is important to handle this chemical with care as it can be harmful if ingested or inhaled and can cause irritation to the skin and eyes.
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 articles and documents
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).
