CAS 93102-05-7

N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine

Description:

N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is an organic compound characterized by its complex structure, which includes a benzylamine core modified with methoxymethyl and trimethylsilylmethyl groups. This compound typically exhibits properties associated with amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility and reactivity. The presence of the trimethylsilyl group enhances its stability and can improve its lipophilicity, making it useful in various chemical applications, including as a protecting group in organic synthesis. Additionally, the methoxymethyl group can serve as a reactive site for further chemical transformations. The compound is likely to be a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. Its applications may extend to pharmaceuticals, agrochemicals, or materials science, where its unique functional groups can be exploited for specific reactivity or interactions. As with any chemical substance, handling should be conducted with care, following appropriate safety protocols due to potential toxicity or reactivity.

Formula: C₁₃H₂₃NOSi

Synonyms:

• N-benzyl(methoxy)-N-((trimethylsilyl)methyl)methanamine
• N-(Methoxymethyl)-N-[(trimethylsilyl)-methyl]-benzylamine
• Benzyl-Methoxymethyl-Trimethylsilanylmethyl-Amine
• N-(Methoxymethyl)-N-[(trimethylsilyl)methyl]-benzenemethanamine
• Benzyl(Methoxymethyl)[(Trimethylsilyl)Methyl]Amine
• N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine

N-Benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine

CAS: 93102-05-7

Formula: C₁₃H₂₃NOSi

Purity: >98.0%(T)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 237.42

Ref: 3B-B1938

N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine, 94%

CAS: 93102-05-7

N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine forms azomethine ylides which readily undergo [3+2] cycloaddition to ,-unsaturated esters affording N-benzyl substituted pyrrolidines in good yields. It reacts with asymmetric 1,3-dipolar cycloadditions in the practical, large-scale synthesis of ch

Formula: C₁₃H₂₃NOSi

Purity: 94%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 237.42

Ref: 02-L19412

N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine

CAS: 93102-05-7

Formula: C₁₃H₂₃NOSi

Purity: 90%

Color and Shape: Liquid

Molecular weight: 237.4133

Ref: IN-DA0035AQ

N-Benzyl-1-methoxy-N-[(trimethylsilyl)methyl]methylamine

CAS: 93102-05-7

N-Benzyl-1-methoxy-N-[(trimethylsilyl)methyl]methylamine

Formula: C₁₃H₂₃NOSi

Purity: 90%

Color and Shape: clear. faint yellow/beige liquid

Molecular weight: 237.41g/mol

Ref: 54-OR43654

N-Benzyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)-amine (tech)

CAS: 93102-05-7

S00978 - N-Benzyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)-amine (tech)

Formula: C₁₃H₂₃NOSi

Purity: 90%

Color and Shape: Liquid, Clear

Molecular weight: 237.418

Ref: 10-S00978

N-(Methoxymethyl)-N-[(trimethylsilyl)methyl]benzenemethanamine (>90%)

Controlled Product

CAS: 93102-05-7

Applications N-(Methoxymethyl)-N-[(trimethylsilyl)methyl]benzenemethanamine is used in the synthesis of pyrrolidine derivatives as novel sodium channel blockers used to treat ischemic related ailments.
References Seki, M. et al.: Bioorg. Med. Chem. Lett., 23, 4230 (2013);

Formula: C₁₃H₂₃NOSi

Purity: >90%

Color and Shape: Neat

Molecular weight: 237.41

Ref: TR-M264620

N-Methoxymethyl-N-Trimethylsilylmethyl-Benzylamine extrapure, 98%

CAS: 93102-05-7

Formula: C₁₃H₂₃NOSi

Molecular weight: 237.41

Ref: SR-13573

N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine

CAS: 93102-05-7

N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is a chiral, electron deficient reagent that reacts with aldehydes and boronic esters to form products with high chemical yields. This compound can be used as a catalyst for acylation reactions, such as the synthesis of p-nitrophenol. N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is synthesized by the reaction of trifluoroacetic acid and an amine, followed by chloroformate displacement. The product is then reacted with acylating agents in the presence of catalysts.

Formula: C₁₃H₂₃NOSi

Purity: Min. 95%

Color and Shape: Clear Colourless To Pale Yellow Liquid

Molecular weight: 237.41 g/mol

Ref: 3D-FM11072