Skip to Content
Merck
All Photos(1)

Documents

423424

Sigma-Aldrich

2-(Trimethylsiloxy)-1,3-cyclohexadiene

95%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H16OSi
CAS Number:
Molecular Weight:
168.31
Beilstein:
2079140
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

form

liquid

refractive index

n20/D 1.462 (lit.)

bp

65 °C/7 mmHg (lit.)

density

0.899 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C[Si](C)(C)OC1=CCCC=C1

InChI

1S/C9H16OSi/c1-11(2,3)10-9-7-5-4-6-8-9/h5,7-8H,4,6H2,1-3H3

InChI key

WPIRVUXAMPRMAY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

2-(Trimethylsiloxy)-1,3-cyclohexadiene ((cyclohexa-1,5-dien-1-yloxy)trimethylsilane) is silyl enol ether of cyclohexenone. The Diels–Alder reactions with dienophiles α-acetoxyacrylonitrile, acrylonitrile and α-chloroacrylonitrile has been studied.

Application

2-(Trimethylsiloxy)-1,3-cyclohexadiene may be used as a diene in the synthesis of isoquinuclidinone 2-aza[2.2.2]octa-3,5-dione by reacting with p-toluenesulfonyl cyanide.

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

116.6 °F - closed cup

Flash Point(C)

47 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Safety Assessment of Diels-Alder Reactions with Highly Reactive Acrylic Monomers.
Abele S, et al.
Organic Process Research & Development, 16(12), 2015-2020 (2012)
High-Temperature Diels-Alder Reactions: Transfer from Batch to Continuous Mode.
Abele S, et al.
Organic Process Research & Development, 16(5), 1114-1120 (2011)
Design and Scale-Up of Diels-Alder Reactions for the Practical Synthesis of 5-Phenylbicyclo [2.2. 2] oct-5-en-2-one.
Funel JA, et al.
Organic Process Research & Development, 15(6), 1420-1427 (2011)
Cynthia K McClure et al.
The Journal of organic chemistry, 68(21), 8256-8257 (2003-10-11)
The hetero-Diels-Alder reaction of an electron-deficient nitrile, p-toluenesulfonyl cyanide, with the silyl enol ether of cyclohexenone produced a hydrolytically sensitive [4 + 2] adduct in good yield. Use of Mander's reagent, ethyl cyanoformate, with the same diene, produced an unstable

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