CAS 68733-63-1

N-benzidril-silil-N-metil-metanamina

Descrição:

N-benzidril-silil-N-metil-metanamina é um composto químico caracterizado por sua estrutura única, que inclui um grupo silano, uma parte benzhidril e um componente de metilamina. Este composto normalmente exibe propriedades associadas tanto a aminas orgânicas quanto a silanos, como reatividade potencial em reações de substituição nucleofílica e a capacidade de formar ligações siloxano. Pode ser utilizado em várias aplicações, incluindo síntese orgânica e como reagente em reações químicas devido aos seus grupos funcionais. A presença do grupo benzhidril pode aumentar sua lipofilicidade, influenciando potencialmente sua solubilidade e interação com sistemas biológicos. Além disso, o composto pode exibir propriedades estereoisoméricas específicas dependendo de sua conformação. As fichas de dados de segurança devem ser consultadas para diretrizes de manuseio e armazenamento, uma vez que compostos dessa natureza podem representar riscos à saúde se não forem gerenciados adequadamente. No geral, N-benzidril-silil-N-metil-metanamina representa um composto versátil no campo da 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%

Cor e Forma: Straw Liquid

Peso molecular: 232.78

Ref: 3H-SID4552.5