structure of N,N-Diethyl-1,1,1-trimethylsilylamine

N,N-Diethyl-1,1,1-trimethylsilylamine

CAS No.: 996-50-9
M. Wt: 145.318
M. Fa: C7H19NSi
InChI Key: JOOMLFKONHCLCJ-UHFFFAOYSA-N
Appearance: Colorless to Light yellow clear liquid

Names and Identifiers of N,N-Diethyl-1,1,1-trimethylsilylamine

CAS Number

996-50-9

EC Number

213-637-6

MDL Number

MFCD00009040

IUPAC Name

N-ethyl-N-trimethylsilylethanamine

InChI

InChI=1S/C7H19NSi/c1-6-8(7-2)9(3,4)5/h6-7H2,1-5H3

InChIKey

JOOMLFKONHCLCJ-UHFFFAOYSA-N

Canonical SMILES

CCN(CC)[Si](C)(C)C

UNII

5LP9WK7P33

UNSPSC Code

12352100

Physical and chemical properties of N,N-Diethyl-1,1,1-trimethylsilylamine

Acidity coefficient

11.27±0.70(Predicted)

Boiling Point

126.3±0.0 °C at 760 mmHg

BRN

635718

Density

0.8±0.1 g/cm3

Exact Mass

145.128677

Flash Point

10.0±0.0 °C

Index of Refraction

1.416

LogP

2.01

Melting Point

-10°C

Molecular Formula

C7H19NSi

Molecular Weight

145.318

PSA

3.24000

Sensitivity

Moisture Sensitive

Storage condition

Store at RT.

Vapour density

>1 (vs air)

Vapour Pressure

14.2±0.2 mmHg at 25°C

Water Solubility

decomposes

Safety Information of N,N-Diethyl-1,1,1-trimethylsilylamine

Pictograms

Signal Word

 Danger

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of N,N-Diethyl-1,1,1-trimethylsilylamine

The compound finds various applications in both academic and industrial settings:

  • Organic Synthesis: It is widely used in organic synthesis for introducing trimethylsilyl groups into molecules.
  • Gas Chromatography: Due to its ability to enhance volatility, it is often employed in gas chromatography for analyzing polar compounds.
  • Chemical Research: Its reactivity makes it valuable for studying reaction mechanisms and developing new synthetic pathways.

Interaction Studies of N,N-Diethyl-1,1,1-trimethylsilylamine

Interaction studies involving N,N-Diethyl-1,1,1-trimethylsilylamine primarily focus on its reactivity with other organic compounds. These studies help elucidate its role as a silylating agent and its effectiveness in various chemical transformations. The compound's interactions with electrophiles and nucleophiles are crucial for understanding its utility in synthetic organic chemistry.

Physical sample testing spectrum (NMR) of N,N-Diethyl-1,1,1-trimethylsilylamine

Physical sample testing spectrum (NMR) of N,N-Diethyl-1,1,1-trimethylsilylamine

Retrosynthesis analysis of N,N-Diethyl-1,1,1-trimethylsilylamine

  • Route#1

    Cas:5775-33-7
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    Cas:996-50-9

  • Route#2

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  • Route#3

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    Cas:996-50-9