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Sigma-Aldrich

Dimethylethylsilane

98%

Synonym(s):

Ethyldimethylsilane

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About This Item

Linear Formula:
CH3CH2SiH(CH3)2
CAS Number:
Molecular Weight:
88.22
Beilstein/REAXYS Number:
1730881
EC Number:
MDL number:
UNSPSC Code:
12352103
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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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.

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

-29.2 °F - closed cup

flash_point_c

-34 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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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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