Structure

Ethyldimethylsilane

CAS
758-21-4
Catalog Number
ACM758214
Category
Alkyl Silane
Molecular Weight
88.22 g/mol
Molecular Formula
C4H12Si

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Specification

Synonyms
Silane,ethyldimethyl-Ethyl(Dimethyl)Silyl
IUPAC Name
ethyl(dimethyl)silicon
Canonical SMILES
CC[Si](C)C
InChI Key
KJISMKWTHPWHFV-UHFFFAOYSA-N
Boiling Point
456 °C
Flash Point
<-34 °C
Density
0.668 g/mL
Appearance
Liquid
Application
Ethyldimethylsilane serves as a versatile agent in chemical reactions It acts as a reducing agent facilitating ligand-free carbon-sulfur bond cleavage reactions Additionally Ethyldimethylsilane serves as a promoter in the cycloisomerization of 16-dienes when using a palladium catalyst highlighting its role in enhancing these specific processes
EC Number
212-061-2
Exact Mass
88.07080
Hazard Statements
F,Xi
H-Bond Acceptor
0
H-Bond Donor
0
Packaging
10 g; 100 g;
Safety Description
S16-S26-S33-S36
What is the PubChem CID of Ethyldimethylsilane?

PubChem CID: 6328647

What is the molecular formula of Ethyldimethylsilane?

Molecular Formula: C4H11Si

What is the molecular weight of Ethyldimethylsilane?

Molecular Weight: 87.22 g/mol

What is the InChI of Ethyldimethylsilane?

InChI: InChI=1S/C4H11Si/c1-4-5(2)3/h4H2,1-3H3

What is the InChIKey of Ethyldimethylsilane?

InChIKey: KJISMKWTHPWHFV-UHFFFAOYSA-N

What is the canonical SMILES of Ethyldimethylsilane?

Canonical SMILES: CC[Si](C)C

What is the CAS number of Ethyldimethylsilane?

CAS number: 758-21-4

What is the European Community (EC) Number of Ethyldimethylsilane?

European Community (EC) Number: 212-061-2

What is the DSSTox Substance ID of Ethyldimethylsilane?

DSSTox Substance ID: DTXSID90883561

Is Ethyldimethylsilane a canonicalized compound?

Yes, Ethyldimethylsilane is canonicalized.

Upstream Synthesis Route 1

  • 78-83-1
  • 280757-21-3
  • 758-21-4
  • 3277-26-7

Reference: [1] Russian Journal of General Chemistry, 2000, vol. 70, # 6, p. 885 - 888

Downstream Synthesis Route 1

  • 100-42-5
  • 758-21-4
  • 18028-01-8

Reference: [1]Rubin, Michael; Schwier, Todd; Gevorgyan, Vladimir
[Journal of Organic Chemistry, 2002, vol. 67, # 6, p. 1936 - 1940]
[2]Green,M. et al.
[Journal of the Chemical Society. Chemical communications, 1976, p. 671 - 672]
Green,M. et al.
[Journal of the Chemical Society, Dalton Transactions, 1977, p. 1519 - 1525]
[3]Sunada, Yusuke; Noda, Daisuke; Soejima, Hiroe; Tsutsumi, Hironori; Nagashima, Hideo
[Organometallics, 2015, vol. 34, # 12, p. 2896 - 2906]

Downstream Synthesis Route 2

  • 758-21-4
  • 13688-56-7
  • 13688-85-2

Reference: [1]Mironov,V.F.; Fedotov,N.S.
[Chemistry of Heterocyclic Compounds, 1966, vol. 2, p. 334 - 337][Khimiya Geterotsiklicheskikh Soedinenii, 1966, vol. 2, p. 453 - 456]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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