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A14405

Sigma-Aldrich

1-Acetyl-1-cyclohexene

97%

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About This Item

Linear Formula:
C6H9COCH3
CAS Number:
932-66-1
Molecular Weight:
124.18
EC Number:
213-256-5
MDL number:
MFCD00001547
UNSPSC Code:
12352100
PubChem Substance ID:
24890545
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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

150.8 °F - closed cup

Flash Point(C)

66 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ0988
STBJ3744
STBB3146
STBB3146V
03510ME

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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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