CAS 68733-63-1

N-benzidril-silil-N-metil-metanamina

Descrizione:

N-benzidril-silil-N-metil-metanamina è un composto chimico caratterizzato dalla sua struttura unica, che include un gruppo silano, una parte benzhidril e un componente di metilamina. Questo composto tipicamente mostra proprietà associate sia alle ammine organiche che ai silani, come la reattività potenziale nelle reazioni di sostituzione nucleofila e la capacità di formare legami silossanici. Può essere utilizzato in varie applicazioni, inclusa la sintesi organica e come reagente in reazioni chimiche grazie ai suoi gruppi funzionali. La presenza del gruppo benzhidril può migliorare la sua lipofilia, influenzando potenzialmente la sua solubilità e interazione con i sistemi biologici. Inoltre, il composto può mostrare specifiche proprietà stereochimiche a seconda della sua conformazione. Le schede di sicurezza devono essere consultate per le linee guida di manipolazione e stoccaggio, poiché composti di questa natura possono comportare rischi per la salute se non gestiti correttamente. In generale, N-benzidril-silil-N-metil-metanamina rappresenta un composto versatile nel campo della chimica sintetica.

Formula: 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

Sinonimi:

• 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

Formula: C₁₅H₁₉NSi

Purezza: 97%

Colore e forma: Straw Liquid

Peso molecolare: 232.78

Ref: 3H-SID4552.5