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Safety Information

362824

Sigma-Aldrich

Acetyltrimethylsilane

97%

Synonym(s):

1-(Trimethylsilyl)ethanone

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About This Item

Linear Formula:
(CH3)3SiCOCH3
CAS Number:
Molecular Weight:
116.23
Beilstein:
2071361
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.411 (lit.)

density

0.811 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(=O)[Si](C)(C)C

InChI

1S/C5H12OSi/c1-5(6)7(2,3)4/h1-4H3

InChI key

REDWSDBFBCDPNI-UHFFFAOYSA-N

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General description

Acetyltrimethylsilane is an organosilicon compound that is commonly used as a protective agent for alcohols and amines in organic synthesis. It is also used as a reagent in various reactions, which includes trimethylsilylation, condensation, carbon-carbon bond formation, and reductive amination reactions.

Application

Acetyltrimethylsilane can be used as a reagent in the synthesis of dihydrophenanthrenes via a C-C insertion reaction. It is also used as a source of carbanion in the synthesis of unsymmetrical biaryls by carbanion-induced ring transformation of 2H-pyran-2-ones under mild basic conditions.

Pictograms

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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 3

Flash Point(F)

46.4 °F - closed cup

Flash Point(C)

8 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

JAN Code

362824-VAR:
362824-BULK:
362824-5G:
362824-1G:
362824-25G:


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Tetrahedron Letters, 26, 6285-6285 (1985)
Xiao-Hong Chen et al.
PloS one, 9(4), e94543-e94543 (2014-04-18)
A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5-fold with an overall yield of 0.4% by purification. The enzyme showed a homotetrameric

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