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538493

Sigma-Aldrich

cis-2-Hexene

95%

Synonym(s):

(2Z)-2-Hexene, (Z)-2-Hexene

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About This Item

Linear Formula:
CH3CH2CH2CH=CHCH3
CAS Number:
7688-21-3
Molecular Weight:
84.16
Beilstein/REAXYS Number:
1719019
EC Number:
231-697-1
MDL number:
MFCD00066520
UNSPSC Code:
12352100
PubChem Substance ID:
24878336
NACRES:
NA.22

Quality Level

100

assay

95%

refractive index

n20/D 1.396 (lit.)

bp

68-70 °C (lit.)

density

0.669 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCC\C=C/C

InChI

1S/C6H12/c1-3-5-6-4-2/h3,5H,4,6H2,1-2H3/b5-3-

InChI key

RYPKRALMXUUNKS-HYXAFXHYSA-N

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General description

cis-2-Hexene is one of the isomeric forms of hexene. It is obtained from 2-hexyne, via semihydrogenation in the presence of Pd78(phen) [phen = 1,10-Phenanthroline] on titanium dioxide in n-octane. cis-2-Hexene is formed as one of the primary product from the dimerization of propylene in the presence of a nickel oxide-silica-alumina catalyst. It undergoes isomerization/hydrosilylation reaction with phenyl silane in the presence of cobalt catalyst to afford 1-hexylphenylsilane.

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pictograms

FlameExclamation mark
GHS02,GHS07

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Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

-13.0 °F - closed cup

flash_point_c

-25 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ2269
MKCL6936
MKCJ7868
MKCG3334
MKCF3406

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Rapid, Regioconvergent, Solvent-Free Alkene Hydrosilylation with a Cobalt Catalyst.
Chen C, et al.
Journal of the American Chemical Society, 137(41), 13244-13247 (2015)
The dimerization of propylene over a nickel oxide-silica-alumina catalyst.
Imai H, et al.
Bulletin of the Chemical Society of Japan, 41(1), 45-48 (1968)
Synthesis and catalytic properties of large ligand stabilized palladium clusters.
Schmid G, et al.
J. Mol. Catal. A: Chem., 107(1), 95-104 (1996)
Chiara Giorio et al.
Faraday discussions, 200, 559-578 (2017-06-06)
Ozonolysis of alkenes is a key reaction in the atmosphere, playing an important role in determining the oxidising capacity of the atmosphere and acting as a source of compounds that can contribute to local photochemical "smog". The reaction products of
Sören Reinhard et al.
ChemMedChem, 12(17), 1464-1470 (2017-07-18)
Cationic lipo-oligomers containing unsaturated oleic acid are potent siRNA carriers based on electrostatic and hydrophobic lipo-polyplex formation and endosomal membrane destabilization. Lipo-oligomers can be produced by solid-phase-supported synthesis in sequence-defined form. However, the trifluoroacetic acid (TFA)-mediated removal of acid-labile protecting
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