62399-01-3

Basic information

• Product Name: Disiloxane, 1,3-dicyclohexyl-1,1,3,3-tetramethyl-
• CAS NO: 62399-01-3
• Molecular Formula: C16H34OSi2
• Molecular Weight: 298.616
• Mol File: 62399-01-3.mol

Chemical Properties

• CAS DataBase Reference: Disiloxane, 1,3-dicyclohexyl-1,1,3,3-tetramethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Disiloxane, 1,3-dicyclohexyl-1,1,3,3-tetramethyl-(62399-01-3)
• EPA Substance Registry System: Disiloxane, 1,3-dicyclohexyl-1,1,3,3-tetramethyl-(62399-01-3)

Safety Data

• Hazardous Substances Data: 62399-01-3(Hazardous Substances Data)

Upstream product

• 4353-77-9 chlorosulfonate de trimethylsilyle 
• 10151-74-3 cyclohexyl-trimethyl-silane 
• 71864-47-6 chloro-cyclohexyl-dimethylsilane 
• 274676-43-6 cyclohexyldimethylsilanol 
• 62381-70-8 C₉H₂₀O₃SSi 
• 75-36-5 acetyl chloride 
• 542-18-7 cyclohexyl chloride 
• 29681-56-9 cyclohexyldimethylsilane 

Relevant articles and documents

Nickel(0) catalyzed oxidation of organosilanes to disiloxanes by air as an oxidant

We report here an efficient non-aqueous route to symmetrical disiloxanes from their corresponding organosilanes using Ni(COD)2 with 3,4,7,8-tetramethyl-1,10-phenanthroline in air. Our methodology is very simple and high yielding. The reaction mechanism is also proposed.

Supported gold nanoparticle catalyst for the selective oxidation of silanes to silanols in water

Hydroxyapatite-supported gold nanoparticles (AuHAP) can act as highly efficient and reusable catalysts for the oxidation of diverse silanes into silanols in water; this is the first catalytic methodology for the selective synthesis of aliphatic silanols using water under organic-solvent-free conditions.

Process of producing a silanic or siloxanic compound containing at least one cycloalkyl ring

A process of producing a silanic or siloxanic compound containing at least one cycloalkyl ring by hydrogenation of a corresponding compound containing at least one aromatic ring, in solution, in the presence of a catalyst comprising palladium, supported on active carbon and at a pressure equal to or higher than 10 bar.

Process for producing a silane or siloxane compound containing a cycloalkyl ring

A process for producing a silane or siloxane compound containing at least one cycloalkyl ring by hydrogenation of a corresponding derivative containing at least one aromatic ring in the presence of a Raney nickel catalyst modified with chromium.

A process for producing a silanic or siloxanic compound containing at least one cycloalkylic ring

A process for producing a silanic or siloxanic compound containing at least one cycloalkylic ring by hydrogenation of a corresponding particularly defined derivative containing at least one aromatic ring in the presence of a Raney nickel catalyst modified with chromium.

A process of producing a silanic or siloxanic compound containing at least one cycloalkyl ring

A process of producing a silanic or siloxanic compound containing at least one cycloalkyl ring by the hydrogenation of a corresponding compound containing at least one aromatic ring, in the presence of a Raney nickel catalyst having a granulometry comprised essentially between 10 and 150 micrometers and a surface area of at least 80 m2/g.

Influence de la taille du cycle sur la substitution electrophile des cycloalkyltrimethylsilanes. Synthese de cycloalkyldimethylfluorosilanes

Cycloalkyltrimethylsilanes, excepting cyclopropyl-, react with electrophiles by Si - Me bond splitting.Consequently silicon can be functionalized by this route.We also propose a new synthesis of cycloalkyldimethylfluoro(or chloro-)silanes.In the case of five or six member ring derivates, the observed results are interpreted by a mechanism involving initial abstraction of hydride ion from the silicon substrate.