18402-10-3 Usage
Description
(Decyloxy)trimethylsilane, with the chemical formula C13H32OSi, is an organosilicon compound that exists as a colorless liquid at room temperature and has a faint odor. It is known for its versatile applications in various chemical and industrial processes due to its unique properties.
Uses
Used in Organic Synthesis:
(Decyloxy)trimethylsilane is used as a silylation reagent for the protection of hydroxyl groups in organic synthesis. This application is crucial in preventing unwanted reactions and ensuring the selective functionalization of specific groups in a molecule.
Used in Electronics Industry:
In the electronics industry, (Decyloxy)trimethylsilane serves as a surface modifier. Its ability to alter the properties of surfaces makes it valuable in the development and manufacturing of electronic components and devices.
Used in Sealants:
(Decyloxy)trimethylsilane is also utilized as a sealant in silicone-based adhesives. Its compatibility with silicone materials and its ability to form strong bonds contribute to its effectiveness in this application.
Used in Production of Organosilicon Compounds:
(DECYLOXY)TRIMETHYLSILANE can be used as a building block in the synthesis of other organosilicon compounds, which have a wide range of applications in various industries, including automotive, construction, and personal care.
Used as a Solvent:
(Decyloxy)trimethylsilane's properties also make it suitable for use as a solvent in different industrial applications. Its ability to dissolve a variety of substances and its compatibility with various materials make it a valuable asset in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 18402-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,0 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18402-10:
(7*1)+(6*8)+(5*4)+(4*0)+(3*2)+(2*1)+(1*0)=83
83 % 10 = 3
So 18402-10-3 is a valid CAS Registry Number.
InChI:InChI=1S/C13H30OSi/c1-5-6-7-8-9-10-11-12-13-14-15(2,3)4/h5-13H2,1-4H3
18402-10-3Relevant articles and documents
New approach to the synthesis of phosphorodichloridites, phosphorochloridites, and trialkyl phosphites
Majewski, Piotr
experimental part, p. 942 - 955 (2010/01/17)
Different trivalent organophosphorus esters such as phosphorodichloridites, phosphorochloridites, and mixed trialkyl phosphites have been easily synthesized in good yields using a HCl-catalyzed reaction of the corresponding chlorophosphine and alkoxytrimethylsilane by mutual exchange of the alkoxy and chlorine ligand pIIICl/ROSiR′3; exchange reaction). Chemoselectivity of the exchange reaction with primary and secondary alkoxytrimethylsilanes, as well as with alkoxytrimethylsilanes and thioalkoxytrimethylsilanes, respectively, has also been examined. It has been also found that the substitution reaction of chlorophosphines with secondary amine occurs more rapidly than the exchange reaction with ROSiR′ 3.
A novel efficient method for the silylation of alcohols using hexamethyldisilazane in an ionic liquid
Mojtahedi, Mohammad M.,Abbasi, Hassan,Abaee, M. Saeed
, p. 1541 - 1544 (2007/10/03)
Benzylic and primary alcohols were protected by hexamethyldisilazane in good to excellent yields at r.t. in 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4]) ionic liquid. In addition, the ionic liquid was recovered quantitatively and reused efficiently in the next reactions. The protocol was successfully applied to the protection of phenols. Copyright Taylor & Francis Group, LLC.
A novel regioselective desulfation method specific to silyl ester of primary sulfate using silylating agents. Selective preparation of secondary alkyl sulfates having a primary hydroxy group
Horibe,Oshita
, p. 181 - 182 (2007/10/03)
The treatment of bis(trimethylsilyl)ester of 1-O-Decylglycerol-2,3-Disulfate with trimethylsilyl-N-trimethylsilylacetimidate (BSA) or (dimethylamino)trimethylsilane caused regioselective desulfation to afford 1-O-decyl glycerol-2-sulfate selectively in good yield. Silylating agents, having nitrogen, seems to be responsible for facilitating trimethylsiloxysulfonyl cation transfer.
