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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.

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’.

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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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