Skip to Content
Merck
CN

254398

4-(Trimethylsiloxy)-3-penten-2-one

97%

Synonym(s):

Acetylacetone enol trimethylsilyl ether, TMS acac

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
(CH3)3SiOC(CH3)=CHCOCH3
CAS Number:
Molecular Weight:
172.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-252-5
Beilstein/REAXYS Number:
1759078
MDL number:
Assay:
97%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

FBADCSUQBLLAHW-SOFGYWHQSA-N

InChI

1S/C8H16O2Si/c1-7(9)6-8(2)10-11(3,4)5/h6H,1-5H3/b8-6+

SMILES string

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

assay

97%

bp

66-68 °C/4 mmHg (lit.)

density

0.912 g/mL at 25 °C (lit.)

functional group

ketone

storage temp.

2-8°C

Looking for similar products? Visit Product Comparison Guide

Application

4-(Trimethylsiloxy)-3-penten-2-one (trimethylsilyl ether of acetylacetone) has been used in the synthesis of isomers of organosilicon carbofunctional compounds:
  • 4-(3′-triethoxysilylpropylimino)pent-2-en-2-ol
  • 4-(3′-triethoxysilylpropylamino)pent-3-en-2-one

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Functionalized silicon-containing imino enols and enamino ketones prepared by hydrolytic condensation.
Semenov VV, et al.
Russian Journal of Applied Chemistry, 80(4), 647-653 (2007)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service