Merck
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281123

Sigma-Aldrich

Dimethylethylsilane

98%

Synonym(s):
Ethyldimethylsilane
Linear Formula:
CH3CH2SiH(CH3)2
CAS Number:
Molecular Weight:
88.22
Beilstein:
1730881
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

6.05 psi ( 20 °C)

Assay

98%

form

liquid

refractive index

n20/D 1.378 (lit.)

bp

44-46 °C (lit.)

density

0.668 g/mL at 25 °C (lit.)

SMILES string

CC[SiH](C)C

InChI

1S/C4H12Si/c1-4-5(2)3/h5H,4H2,1-3H3

InChI key

QGBMSFLTRRZTGI-UHFFFAOYSA-N

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1 of 4

This Item
282588409987808725
Dimethylethylsilane 98%

Sigma-Aldrich

281123

Dimethylethylsilane

Diethylmethylsilane 95%

Sigma-Aldrich

282588

Diethylmethylsilane

refractive index

n20/D 1.378 (lit.)

refractive index

n20/D 1.398 (lit.)

refractive index

n20/D 1.448 (lit.)

refractive index

n/D 1.462

bp

44-46 °C (lit.)

bp

78 °C (lit.)

bp

196 °C (lit.)

bp

-

density

0.668 g/mL at 25 °C (lit.)

density

0.705 g/mL at 25 °C (lit.)

density

0.968 g/mL at 25 °C (lit.)

density

0.968 g/mL at 25 °C

vapor pressure

6.05 psi ( 20 °C)

vapor pressure

-

vapor pressure

-

vapor pressure

-

form

liquid

form

liquid

form

-

form

liquid

Application

Dimethylethylsilane can be used as:
  • A reducing agent in the ligand-free carbon-sulfur bond cleavage reaction.
  • A promoter in cycloisomerization of 1,6-dienes using palladium catalyst.

accessory

Product No.
Description
Pricing

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(C)

-34 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Development, synthetic scope, and mechanistic studies of the palladium-catalyzed cycloisomerization of functionalized 1, 6-dienes in the presence of silane
Kisanga P and Widenhoefer RA
Journal of the American Chemical Society, 122(41), 10017-10026 (2000)
Nekane Barbero et al.
Organic letters, 14(3), 796-799 (2012-01-20)
A catalytic reductive cleavage of C(sp(2))- and C(sp(3))-SMe bonds under ligandless conditions is presented. The method is characterized by its wide scope and high chemoselectivity profile including challenging substrate combinations, allowing the design of orthogonal and site-selectivity approaches.

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