assay
98%
form
solid
mp
88-91 °C (lit.)
functional group
ketone, phenyl
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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 461229-5G | 04061832619323 |
| 461229-25G | 04061832619316 |