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About This Item
Linear Formula:
C6H9COCH3
CAS Number:
Molecular Weight:
124.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
form
liquid
refractive index
n20/D 1.49 (lit.)
bp
201-202 °C (lit.)
density
0.966 g/mL at 25 °C (lit.)
SMILES string
CC(=O)C1=CCCCC1
InChI
1S/C8H12O/c1-7(9)8-5-3-2-4-6-8/h5H,2-4,6H2,1H3
InChI key
LTYLUDGDHUEBGX-UHFFFAOYSA-N
WGK
WGK 3
Flash Point(F)
150.8 °F
Flash Point(C)
66 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Marcelina Mazur et al.
Biomolecules, 10(1) (2020-01-16)
Starting from 1-acetyl-1-cyclohexene, three enantiomeric pairs (ee ≥99%) of bicyclic δ-halo-γ-lactones with cyclohexane ring were obtained in five-step synthesis. The key stereochemical steps were lipase-catalyzed kinetic resolution of racemic 1-(cyclohex-1-en-1-yl) ethanol followed by transfer of chirality to ethyl 2-(2-ethylidenecyclohexyl) acetate
Gilles Brackman et al.
PloS one, 6(1), e16084-e16084 (2011-01-21)
Many bacteria, including Vibrio spp., regulate virulence gene expression in a cell-density dependent way through a communication process termed quorum sensing (QS). Hence, interfering with QS could be a valuable novel antipathogenic strategy. Cinnamaldehyde has previously been shown to inhibit
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