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N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine, 94%, Thermo Scientific Chemicals
製品番号（カタログ番号）： L19412.03
1 g, Each
化学物質識別子
CAS
93102-05-7
IUPAC Name
benzyl(methoxymethyl)[(trimethylsilyl)methyl]amine
Molecular Formula
C13H23NOSi
InChI Key
RPZAAFUKDPKTKP-UHFFFAOYSA-N
SMILES
COCN(CC1=CC=CC=C1)C[Si](C)(C)C
仕様
スペックシートAppearance (Color)
Clear, colorless to pale yellow
Assay (Non-aqueous acid-base Titration)
>92.5%
Refractive Index
1.4885-1.4955 @ 20?C
Form
Liquid
Proton NMR
Conforms to structure
概要
N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine forms azomethine ylides which readily undergo [3+2] cycloaddition to α,β-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 chiral pyrrolidines. It is used in the the synthesis of 3-carboxy-1-azabicyclo[2.2.1]heptane derivatives, an important class of physiologically active compounds.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine forms azomethine ylides which readily undergo [3+2] cycloaddition to α,ß-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 chiral pyrrolidines. It is used in the the synthesis of 3-carboxy-1-azabicyclo[2.2.1]heptane derivatives, an important class of physiologically active compounds.
Solubility
Soluble in chloroform, ethyl acetate.
Notes
Moisture & Light Sensitive. Store away from oxidizing agents.
N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine forms azomethine ylides which readily undergo [3+2] cycloaddition to α,ß-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 chiral pyrrolidines. It is used in the the synthesis of 3-carboxy-1-azabicyclo[2.2.1]heptane derivatives, an important class of physiologically active compounds.
Solubility
Soluble in chloroform, ethyl acetate.
Notes
Moisture & Light Sensitive. Store away from oxidizing agents.
RUO – Research Use Only
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