Skip to Content
Merck
All Photos(2)

Documents

424714

Sigma-Aldrich

2,6-Diphenylcyclohexanone, mixture of cis and trans

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C6H5)2C6H8(=O)
CAS Number:
Molecular Weight:
250.33
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

119-121 °C (lit.)

SMILES string

O=C1C(CCCC1c2ccccc2)c3ccccc3

InChI

1S/C18H18O/c19-18-16(14-8-3-1-4-9-14)12-7-13-17(18)15-10-5-2-6-11-15/h1-6,8-11,16-17H,7,12-13H2

InChI key

JHMUMWBKYPMOLI-UHFFFAOYSA-N

General description

2,6-Diphenylcyclohexanone is a cyclohexanone with two phenyl substituents at two α-positions. 2,6-Diphenylcyclohexanone is the starting material employed in the synthesis of cis- and trans-2-(p-carboxybenzyl)-2,6-diphenyl-6-vinylcyclohexanone. cis -2,6-Diphenylcyclohexanone is photochemically active and it undergoes photodecarbonylation reactions.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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

Platz MS, et al.
Reviews of Reactive Intermediate Chemistry, 310-312 (2007)
Horspool WM and Lenci F.
CRC Handbook of Organic Photochemistry and Photobiology, 1 -2, 48-48 (2003)
Engineering reactions in crystals: suppression of photodecarbonylation by intramolecular β-phenyl quenching.
Ng D, et al.
Tetrahedron Letters, 42(52), 9113-9116 (2001)

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