CAS 68733-63-1

N-benzhydrylsilyl-N-methyl-methanamine

Description:

N-benzhydrylsilyl-N-methyl-methanamine is a chemical compound characterized by its unique structure, which includes a silane group, a benzhydryl moiety, and a methylamine component. This compound typically exhibits properties associated with both organic amines and silanes, such as potential reactivity in nucleophilic substitution reactions and the ability to form siloxane bonds. It may be utilized in various applications, including organic synthesis and as a reagent in chemical reactions due to its functional groups. The presence of the benzhydryl group can enhance its lipophilicity, potentially influencing its solubility and interaction with biological systems. Additionally, the compound may exhibit specific stereochemical properties depending on its conformation. Safety data sheets should be consulted for handling and storage guidelines, as compounds of this nature can pose health risks if not managed properly. Overall, N-benzhydrylsilyl-N-methyl-methanamine represents a versatile compound in the realm of synthetic chemistry.

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

Synonyms:

• 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

Purity: 97%

Color and Shape: Straw Liquid

Molecular weight: 232.78

Ref: 3H-SID4552.5