Substance
ID:331398
Names and Identifiers
IUPAC Traditional name
benzyl(methoxymethyl)[(trimethylsilyl)methyl]amine
IUPAC name
benzyl(methoxymethyl)[(trimethylsilyl)methyl]amine
Synonyms
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamineN-(甲氧基甲基)-N-(三甲基硅烷基甲基)苄胺
Properties
Product Information
Linear Formula
C6H5CH2N(CH2OCH3)CH2Si(CH3)3
Purity
96%
Physical Property
Boiling Point
76 °C/0.3 mmHg(lit.)
Density
0.928 g/mL at 25 °C(lit.)
Flash Point
66 °C
150.8 °F
Refractive Index
n20/D 1.492(lit.)
Safety Information
MSDS Link
German water hazard class
3
GHS Precautionary statements
P261-P305+P351+P338
Safety Statements
26
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Hazard statements
H315-H319-H335
European Hazard Symbols
Irritant (Xi)Risk Statements
36/37/38
GHS Signal Word
Warning
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Molecule Details
Application
Forms azomethine ylides which readily undergo [3+2] cycloaddition to α,β-unsaturated esters affording N-benzyl substituted pyrrolidines in good yields.1
Reacted in asymmetric 1,3-dipolar cycloadditions in the practical, large-scale synthesis of chiral pyrrolidines.
Packaging
1, 5, 25, 100 g in glass bottle
Forms azomethine ylides which readily undergo [3+2] cycloaddition to α,β-unsaturated esters affording N-benzyl substituted pyrrolidines in good yields.1
Reacted in asymmetric 1,3-dipolar cycloadditions in the practical, large-scale synthesis of chiral pyrrolidines.
Packaging
1, 5, 25, 100 g in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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