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Sigma-Aldrich

5-Hexenyl acetate

97%

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About This Item

Linear Formula:
CH3CO2(CH2)4CH=CH2
CAS Number:
5048-26-0
Molecular Weight:
142.20
MDL number:
MFCD00060856
UNSPSC Code:
12352100
PubChem Substance ID:
24878662
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.423 (lit.)

bp

173-174 °C (lit.)

density

0.883 g/mL at 25 °C (lit.)

SMILES string

CC(=O)OCCCCC=C

InChI

1S/C8H14O2/c1-3-4-5-6-7-10-8(2)9/h3H,1,4-7H2,2H3

InChI key

MPLWNENKBSBMFN-UHFFFAOYSA-N

General description

5-Hexenyl acetate is a linear ester. It can undergo ruthenium-catalyzed cross-metathesis reactions with α-substituted vinyl boronates in dichloromethane. It participates in the post-polymerization modification step during the preparation of poly(vinylnorbornene).

Application

5-Hexenyl acetate may be used in the synthesis of (4E,7Z)-4,7-tridecadienyl acetate.

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

141.1 °F - closed cup

flash_point_c

60.6 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Nonconjugated dienes from 1-alkenes: Application to the synthesis of sex pheromone (4E, 7Z)-4, 7-Tridecadienyl acetate
Kim TH and Park KM
Tetrahedron Letters, 36.27, 4833-4836 (1995)
Ring-opening metathesis polymerization of vinylnorbornene and following polymer modifications
Balcar H, et al.
Journal of Polymer Research, 21.9, 1-8 null
Synthesis of tri-substituted vinyl boronates via ruthenium-catalyzed olefin cross-metathesis
Morrill C, et al.
Tetrahedron Letters, 45.41 , 7733-7736 (2004)
Xuejiao Gao et al.
Nature communications, 9(1), 118-118 (2018-01-11)
It is known that self-assembled molecular monolayer doping technique has the advantages of forming ultra-shallow junctions and introducing minimal defects in semiconductors. In this paper, we report however the formation of carbon-related defects in the molecular monolayer-doped silicon as detected
Xicotencatl Camacho-Coronel et al.
Frontiers in plant science, 11, 121-121 (2020-03-12)
Numerous plant-derived volatile organic compounds (VOCs) induce the expression of resistance-related genes and thereby cause an "associational resistance" in neighbouring plants. However, VOCs can also be sequestered by plant cuticular waxes. In case that they maintain their biological activity, such
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