Skip to Content
Merck
All Photos(1)

Documents

371270

Sigma-Aldrich

2-(3-Methoxyphenyl)cyclohexanone

technical grade, 90%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3OC6H4C6H9(=O)
CAS Number:
Molecular Weight:
204.26
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Assay

90%

form

liquid

refractive index

n20/D 1.546 (lit.)

density

1.1 g/mL at 25 °C (lit.)

SMILES string

COc1cccc(c1)C2CCCCC2=O

InChI

1S/C13H16O2/c1-15-11-6-4-5-10(9-11)12-7-2-3-8-13(12)14/h4-6,9,12H,2-3,7-8H2,1H3

InChI key

KACQSVYTBQDRGP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

2-(3-Methoxyphenyl)cyclohexanone is an aromatic ketone. It is a clear, colorless liquid. 2-(3-Methoxyphenyl)cyclohexanone is reported to participate in the synthesis of 9-azamorphinan.

Application

2-(3-Methoxyphenyl)cyclohexanone may be used as starting reagent for the synthesis of octahydrophenanthrene, an important intermediate in the synthesis of morphinans. It may be used in the synthesis of 2-methyl-5-phenyl morphan.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

Casy AF and Parfitt RT.
Opioid Analgesics: Chemistry and Receptors, 215-215 (1986)
Antitumor agents. 4. Cytotoxicity and in vitro activity of helenalin esters and related derivatives.
K H Lee et al.
Journal of medicinal chemistry, 16(3), 299-301 (1973-03-01)
Casy AF and Parfitt RT.
Opioid Analgesics: Chemistry and Receptors, 142-142 (1986)

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