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461229

Sigma-Aldrich

2-Benzoylcyclohexanone

98%

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About This Item

Linear Formula:
C6H5COC6H9(=O)
CAS Number:
Molecular Weight:
202.25
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

88-91 °C (lit.)

SMILES string

O=C1CCCCC1C(=O)c2ccccc2

InChI

1S/C13H14O2/c14-12-9-5-4-8-11(12)13(15)10-6-2-1-3-7-10/h1-3,6-7,11H,4-5,8-9H2

InChI key

YTVQIZRDLKWECQ-UHFFFAOYSA-N

General description

2-Benzoylcyclohexanone can be prepared from the reaction between silyl enol ether of cyclohexanone and benzoyl fluoride.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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’.

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The regioselective preparation of 1, 3-diketones within a micro reactor.
Wiles C, et al.
Chemical Communications (Cambridge, England), 10, 1034-1035 (2002)
Gilbert E Tumambac et al.
Chirality, 17(4), 171-176 (2005-04-13)
The kinetics of the racemization of 2-benzoylcyclohexanone 1 in hexanes, ethanol, and mixtures thereof have been investigated by time dependence of enantiomeric purity using enantioselective HPLC. In pure hexanes and ethanol, the racemization half-lives were determined as 552 and 23.8

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