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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

A14405-25G:
A14405-BULK:
A14405-VAR:
A14405-5G:
A14405-1KG:

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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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