5833-47-6 Usage
Description
1,1-DIMETHYL-1-SILA-2-OXACYCLOHEXANE, with the molecular formula C6H14OSi, is an organosilicon compound that falls under the category of cyclic siloxanes. It is a colorless liquid with a faint odor and is known for its high flammability. This versatile chemical is integral to the production of silicone polymers and is utilized in a variety of industrial processes. It also serves as a reagent in organic synthesis and as a fundamental building block for the synthesis of more complex silicon-containing molecules. Its applications are extensive, contributing to the manufacturing of a wide array of products, from adhesives and sealants to medical implants and electronic devices.
Uses
Used in Silicone Polymer Production:
1,1-DIMETHYL-1-SILA-2-OXACYCLOHEXANE is used as a key component in the production of silicone polymers for its ability to contribute to the formation of the polymer's backbone, which is essential for the material's unique properties such as heat resistance and flexibility.
Used in Industrial Processes:
In various industries, 1,1-DIMETHYL-1-SILA-2-OXACYCLOHEXANE is used as a reagent or intermediate in the synthesis of other chemicals, facilitating the creation of a range of products that require the specific characteristics of organosilicon compounds.
Used in Organic Synthesis:
As a reagent in organic synthesis, 1,1-DIMETHYL-1-SILA-2-OXACYCLOHEXANE is used to facilitate specific chemical reactions, often providing a pathway to more complex silicon-containing molecules that are otherwise difficult to synthesize.
Used in Manufacturing of Diverse Products:
1,1-DIMETHYL-1-SILA-2-OXACYCLOHEXANE is used as a building block in the manufacturing of a wide array of products, including adhesives and sealants, medical implants, and electronic devices, due to its contribution to the unique properties of silicone-based materials.
Check Digit Verification of cas no
The CAS Registry Mumber 5833-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5833-47:
(6*5)+(5*8)+(4*3)+(3*3)+(2*4)+(1*7)=106
106 % 10 = 6
So 5833-47-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H19N3O4/c1-25-16-11-14(7-8-15(16)22)12-20-21-18(24)17(23)19-10-9-13-5-3-2-4-6-13/h2-8,11-12,20H,9-10H2,1H3,(H,19,23)(H,21,24)
5833-47-6Relevant articles and documents
Process for producing aromatic hydroxy compound
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, (2008/06/13)
A process for producing an aromatic hydroxy compound having hydroxyl group at the para-position with respect to a hydroxy or an alkoxy substituent group present in the aromatic ring at a high yield and at a high selectivity, using a novel and useful hydroxylation catalyst which can afford to introduce hydroxyl group directly into aromatic ring at the para-position with respect to a hydroxy or an alkoxy substituent group, by reacting at least one compound selected from the group consisting of phenols, alkoxybenzenes and derivatives of them with hydrogen peroxide in the presence of the catalyst, wherein the hydroxylation catalyst is constituted of an oleophilized crystalline titanosilicate.
Palladium-catalyzed rearrangement of silanes containing oxygen or halogen α to silicon
Gevorgyan, Vladimir,Borisova, Larisa,Lukevics, Edmunds
, p. 277 - 285 (2007/10/02)
Rearrangements of tetrahydrofuryl- and tetrahydropyranyl-hydrosilanes to oxasilaalkanes, of acetoxymethyl-hydrosilanes to acetoxysilanes, and halogenomethyl-hydrosilanes to halogenosilanes in the presence of palladium catalyst have been studied.The reaction has been shown to proceed more rapidly in tetrahydrofuran and hexane than in benzene or acetonitrile.The progressive replacement of the methyl groups on the silicon atom by phenyl groups slowed down the rearrangement, as did change from five-membered to six-membered heterocycles.
SYNTHESIS OF (ACYLOXYBUTYL)DIMETHYLCHLOROSILANES, BIS(ACYLOXYBUTYL)TETRAMETHYLDISILOXANES, AND THEIR DERIVATIVES
Volkova, L. M.,Makarova, N. N.,Lyakhovetskii, Yu. I.
, p. 1515 - 1518 (2007/10/02)
New bis(acyloxybutyl)tetramethyldisiloxanes and (acyloxybutyl)dimethylchlorosilanes were prepared by reactions of 2,2-dimethyl-1-oxa-2-silacyclohexane with valeric, heptanoic, thioacetic, p-nitrobenzoic, and p-bromobenzoic acids and the corresponding acyl chlorides.Bis(p-aminobenzoyloxybutyl)tetramethyldisiloxane was formed by the reduction of bis(p-nitrobenzoyloxybutyl)tetramethyldisiloxane with hydrazine hydrate.The corresponding methacroyloxy derivatives were isolated by the condensation of (methacroyloxybutyl)dimethylchlorosilane with 2-hydroxy-2,4,4,6,6,8,8-heptamethylcyclotetrasiloxane or 2-hydroxy-4,4,6,6,8,8,10,10,12,12-undecamethylcyclohexasiloxane.The mass spectra of these compounds are given.