Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

543101

Sigma-Aldrich

5-Hexenyl acetate

97%

Sign Into View Organizational & Contract Pricing
All Photos(1)

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.[1] It participates in the post-polymerization modification step during the preparation of poly(vinylnorbornene).[2]

Application

5-Hexenyl acetate may be used in the synthesis of (4E,7Z)-4,7-tridecadienyl acetate.[3]

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)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCP2230
MKBT1716V
MKBK3952V
01110JJ
09020JD

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
Synthesis of tri-substituted vinyl boronates via ruthenium-catalyzed olefin cross-metathesis
Morrill C, et al.
Tetrahedron Letters, 45.41 , 7733-7736 (2004)
Ring-opening metathesis polymerization of vinylnorbornene and following polymer modifications
Balcar H, et al.
Journal of Polymer Research, 21.9, 1-8 null
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
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service