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Usage

Uses

Used in Chemical Synthesis:
1,6-Bis(chlorodimethylsilyl)hexane is used as a reagent in chemical synthesis for its ability to facilitate various organic reactions. Its unique structure allows it to act as an intermediate in the formation of more complex molecules, contributing to the development of new compounds and materials.
Used in Research and Development:
In the field of research and development, 1,6-bis(chlorodimethylsilyl)hexane is employed as a key component in the exploration of new chemical pathways and the synthesis of novel molecules. Its versatility in organic synthesis makes it a valuable tool for chemists working on innovative projects and the advancement of scientific knowledge.
Used in Laboratory Settings:
1,6-Bis(chlorodimethylsilyl)hexane is used as a specialist material in laboratory settings, where it is involved in the preparation and study of various chemical compounds. Its application in controlled environments ensures that researchers can safely and effectively utilize its properties for their experiments and studies.
Used in the Production of Advanced Materials:
1,6-Bis(chlorodimethylsilyl)hexane is used as a precursor in the production of advanced materials, such as polymers and composites, that exhibit unique properties and applications. Its role in the synthesis of these materials contributes to the development of new technologies and industries that rely on innovative materials with enhanced performance characteristics.

InChI:InChI=1/C10H24Cl2Si2/c1-13(2,11)9-7-5-6-8-10-14(3,4)12/h5-10H2,1-4H3

Upstream product

• 75-78-5 dimethylsilicon dichloride 
• 2163-00-0 1,6-dichlorohexane 
• 1066-35-9 dimethylmonochlorosilane 
• 592-42-7 1,5-Hexadien 
• 13083-96-0 1,6-bis(trimethylsilyl)hexane 
• 2062-59-1 1,6-Bis-(fluor-dimethylsilyl)-hexan 

Downstream Products

• 75-77-4 chloro-trimethyl-silane 
• 349586-22-7 [1,6-bis-((4-methyl-1-phenyl-1H-phosphol-3-yl)dimethylsilylmethyl)-hexane]tetradecacarbonyltetrairon 
• 1080555-77-6 C₂₁H₃₇ClOSi₂ 

Relevant academic research and scientific papers

Syntheses, Solid State Structures and Photochemistry of α,ω-Bis-[(1,8-dichloroanthracen-10-yl)dimethylsilyl]alkanes

Starting from 10-bromo-1,8-dichloroanthracene, a series of 1,8-dichlorinated anthracene derivatives, flexibly bridged in position 10 by -Me 2 Si- and -Me 2 Si-(CH 2) n -SiMe 2 - linker units, were synthesised. The linked anthracenes were generated by converting (1,8-dichloroanthracen-10-yl)lithium with chlorosilanes in salt-elimination reactions. The bichromophors were tested in UV light induced photo reactions. None of the new compounds yielded any intra- or intermolecular photoproduct. All α,ω-(dimethylsilyl)alkane-linked bisanthracenes decomposed to give 1,8-dichloro-9-hydroxyanthracen-10(9 H)-one in the presence of oxygen. A completely different behaviour was shown by the bisanthracenyldimethylsilane, undergoing a 9,10:3′,4′-photocyclomerisation reaction. The new compounds were characterised by NMR spectroscopy, mass spectrometry and in most cases by X-ray diffraction studies.

Silicon-containing heterocyclic compounds I. Preparation and reactions of 1,1,2,2,-tetramethyl-1,2-disilacycloalkanes, from disilacyclopentane to disilacyclooctane

Four 1,2-disilacycloalkanes of the formula Me2SiSiMe2-(CH2)n, where n equals 3, 4, 5 and 6, have been prepared by two methods: one involves reaction of ClMe2SiSiMe2Cl with BrMg(CH2)nMgBr, the other comprises sodium/potassium condensation of ClMe2Si(CH2)nSiMe2Cl. It has been found that both the disilacyclopentane and -hexane exclusively undergo cleavage of the silicon-silicon bond when treated with concentrated sulfuric acid, whereas the disilacycloheptane gives several products in which the silicon-silicon bond has not been cleaved. The disilacyclopentane undergoes cleavage of the silicon-silicon bond when heated with 0.6 N sodium ethoxide in ethanol at 90°, while the disilacyclohexane is quite stable under the same conditions.