CAS 2083-91-2: (Dimethylamino)trimethylsilane

N-(Trimethylsilyl)dimethylamine is a reactive, cationic monomer that polymerizes with the help of an initiator and a catalyst. It is used in the production of ferroelectric polymers, which are used for applications such as transistors and memory devices. N-(Trimethylsilyl)dimethylamine has been shown to be able to form heterocyclic aromatic hydrocarbons through the reaction with hydrogen chloride. This process is also known as silylation. N-(Trimethylsilyl)dimethylamine can also be used to generate dihydro derivatives from carbonyl groups by reacting with nitrogen atoms; these derivatives are often found in cavity transfer mechanisms.

N,N-Dimethyltrimethylsilylamine was used in the synthesis of phosphoramidite. It was also employed as a reagent in the preparation of iminium salts and amides as well as for the silylation of polymers. A combination of N-(trimethylsilyl)dimethylamine and MeI was also effective to give p-methylbenzoic acid with a 85% yield based on 90% conversion from the corresponding Me ester. DETA has been treated with N-(trimethylsilyl)-dimethylamine to yield mono-, di- and tri- silylated derivativesThis Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

S06925 - N,N-Dimethylaminotrimethylsilane

N,N-Dimethyltrimethylsilylamine

Trimethylsilyl Blocking Agent Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure. Alkyl Silane - Conventional Surface Bonding Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure. Dimethylaminotrimethylsilane; Pentamethylsilanamine; Trimethylsilyldimethylamine; TMSDMA ΔHvap: 31.8 kJ/molSelectively silylates equatorial hydroxyl groups in prostaglandin synthesisStronger silylation reagent than HMDS; silylates amino acidsDialkylaminotrimethylsilanes are used in the synthesis of pentamethinium saltsWith aryl aldehydes converts ketones to α,β-unsaturated ketonesSimilar to SID6110.0 and SID3398.0Liberates Me2NH upon reactionSilylates urea-formaldehyde polycondensatesSilylates phosphorous acidsNafion SAC-13 has been shown to be a recyclable catalyst for the trimethylsilylation of primary, secondary, and tertiary alcohols in excellent yields and short reaction timesSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure