55724-30-6

Basic information

• Product Name: Silane, [1,4-cyclohexanediylbis(oxy)]bis[trimethyl-
• Synonyms: Silane, [1,4-cyclohexanediylbis(oxy)]bis[trimethyl-;1,4-Cyclohexanediylbis(oxy)bis(trimethylsilane);Cyclohexane-1,4-diylbis(oxy)bis(trimethylsilane)
• CAS NO: 55724-30-6
• Molecular Formula: C₁₂H₂₈O₂Si₂
• Molecular Weight: 260.52
• Mol File: 55724-30-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Silane, [1,4-cyclohexanediylbis(oxy)]bis[trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, [1,4-cyclohexanediylbis(oxy)]bis[trimethyl-(55724-30-6)
• EPA Substance Registry System: Silane, [1,4-cyclohexanediylbis(oxy)]bis[trimethyl-(55724-30-6)

Safety Data

• Hazardous Substances Data: 55724-30-6(Hazardous Substances Data)

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 556-48-9 1,4-Cyclohexanediol 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 

Downstream Products

• 556-48-9 1,4-Cyclohexanediol 

Relevant articles and documents

Boric acid as cost-effective and recyclable catalyst for trimethylsilyl protection and deprotection of alcohols and phenols

Boric acid has been used as a green, selective and recyclable catalyst for trimethysilylation of alcohols and phenols using hexamethyldisilazane in acetonitrile. Deprotection of trimethylsilyl ethers to their parent alcohols and phenols was also achieved using this catalyst in water at room temperature. The salient features of this methodology are cheap processing, mild acidity conditions, excellent yields of products and easy availability of the catalyst.

Novel and highly effective method for the trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS), catalyzed by I2 generated in situ using Fe(NO3)3 · 9 H 2O/NaI under heterogeneous and neutral conditions

Structurally diverse alcohols and phenols were trimethylsilylated in a clean and efficient reaction with hexamethyldisilazane (HMDS) based on the use of I2 generated in situ from Fe(NO3)3 · 9 H2O/NaI. The reaction occurs very rapid in good-to-high yield in CH2Cl2 at room temperature, and the use of toxic and corrosive molecular I2 is avoided.

Mild and highly efficient method for the silylation of alcohols using hexamethyldisilazane catalyzed by iodine under nearly neutral reaction conditions

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