CAS 68733-63-1

N-bencilhidril-silil-N-metil-metanamina

Descripción:

N-bencilhidril-silil-N-metil-metanamina es un compuesto químico caracterizado por su estructura única, que incluye un grupo silano, una parte benzhidril y un componente de metilamina. Este compuesto típicamente exhibe propiedades asociadas tanto con aminas orgánicas como con silanos, como la reactividad potencial en reacciones de sustitución nucleofílica y la capacidad de formar enlaces siloxano. Puede ser utilizado en diversas aplicaciones, incluida la síntesis orgánica y como reactivo en reacciones químicas debido a sus grupos funcionales. La presencia del grupo benzhidril puede mejorar su lipofilia, influyendo potencialmente en su solubilidad e interacción con sistemas biológicos. Además, el compuesto puede exhibir propiedades estereoquímicas específicas dependiendo de su conformación. Se deben consultar las hojas de datos de seguridad para las pautas de manejo y almacenamiento, ya que los compuestos de esta naturaleza pueden representar riesgos para la salud si no se gestionan adecuadamente. En general, N-bencilhidril-silil-N-metil-metanamina representa un compuesto versátil en el ámbito de la química sintética.

Fórmula: C₁₅H₁₉NSi

InChI: InChI=1/C15H19NSi/c1-16(2)17-15(13-9-5-3-6-10-13)14-11-7-4-8-12-14/h3-12,15H,17H2,1-2H3

SMILES: CN(C)[SiH2]C(c1ccccc1)c1ccccc1

Sinónimos:

• Silanamine, N,N,1-trimethyl-1,1-diphenyl-
• N-benzhydrylsilyl-N-methyl-methanamine
• DIPHENYLMETHYL(DIMETHYLAMINO)SILANE

(DIPHENYL)METHYL(DIMETHYLAMINO)SILANE

CAS: 68733-63-1

Phenyl-Containing 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.
Aromatic 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.
Diphenylmethyl(dimethylamino)silane; N,N,1-Trimethyl-1,1-diphenylsilanamine
More reactive than SID4552.0Liberates dimethylamine upon reactionSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure

Fórmula: C₁₅H₁₉NSi

Pureza: 97%

Forma y color: Straw Liquid

Peso molecular: 232.78

Ref: 3H-SID4552.5