Skip to Content
Merck
All Photos(1)

Key Documents

541176

Sigma-Aldrich

Cyclohexyl phenyl ether

95%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5OC6H11
CAS Number:
Molecular Weight:
176.25
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

refractive index

n20/D 1.525 (lit.)

bp

127-128 °C/15 mmHg (lit.)

density

1.078 g/mL at 25 °C (lit.)

functional group

phenoxy

SMILES string

C1CCC(CC1)Oc2ccccc2

InChI

1S/C12H16O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12H,2,5-6,9-10H2

InChI key

OSAOIDIGMBDXED-UHFFFAOYSA-N

General description

Cyclohexyl phenyl ether is an alkyl aryl ether. It undergoes thermolysis and aquathermolysis reactions to yield 1-methylcyclopentene and phenol as major products. Cyclohexyl phenyl ether can be synthesized from cyclohexyl bromide and phenol. It can also be prepared from 2-cyclohexen-1-one via oxidative aromatization in the presence of VO(OEt)Cl2 and cyclohexanol.

Pictograms

FlameExclamation mark

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)

64.9 °F - closed cup

Flash Point(C)

18.3 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Comparative study of phenol alkylation mechanisms using homogeneous and silica-supported boron trifluoride catalysts.
Wilson K, et al.
J. Mol. Catal. A: Chem., 159(2), 309-314 (2000)
Aqueous organic chemistry. 3. Aquathermolysis: reactivity of ethers and esters.
Siskin M, et al.
Energy and Fuels, 4(5), 488-492 (1990)
VO (OR) Cl2-induced oxidative aromatization of α,β-unsaturated cyclohexenones.
Hirao T, et al.
The Journal of Organic Chemistry, 55(1), 358-360 (1990)

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