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About This Item
Linear Formula:
H2C=CHCH2CH2CH=CH2
CAS Number:
Molecular Weight:
82.14
Beilstein:
1731106
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor pressure
367 mmHg ( 37.7 °C)
Quality Level
Assay
97%
form
liquid
contains
Contains ~100ppm BHT as stabilizer
refractive index
n20/D 1.404 (lit.)
bp
60 °C (lit.)
mp
−141 °C (lit.)
density
0.692 g/mL at 25 °C (lit.)
functional group
allyl
storage temp.
2-8°C
SMILES string
C=CCCC=C
InChI
1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2
InChI key
PYGSKMBEVAICCR-UHFFFAOYSA-N
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Related Categories
Application
1,5-Hexadiene was used to study the Pd(II)-catalyzed cycloisomerization of functionalized 1,5-hexadienes.
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
-16.6 °F - closed cup
Flash Point(C)
-27 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Amber L Russell et al.
International journal of mass spectrometry, 287(1-3), 8-15 (2010-04-20)
A method for the study of reactions of open-shell neutrals (radicals) and radical cations is described. Pyrolysis (25-1500 degrees C) of thermally labile compounds, such as, 1,5-hexadiene via a Chen nozzle yields a seeded beam of reactive species in helium.
Björn Nelson et al.
Organic letters, 13(16), 4438-4441 (2011-07-29)
Scope and limitations of the Pd(II)-catalyzed cycloisomerization of functionalized 1,5-hexadienes have been studied. In situ NMR experiments indicate a challenging competition between various reaction pathways. A careful balance between substrate structure, nature of the precatalyst, and reaction conditions was required
Richard G Closser et al.
ACS applied materials & interfaces, 11(24), 21988-21997 (2019-06-11)
The synthesis of an all-carbon backboned fluoropolymer using photoactivated molecular layer deposition (pMLD) is developed. pMLD is a vapor-phase, layer-by-layer, organic thin film synthesis method utilizing UV light, allowing for the creation of materials previously unavailable via thermal MLD. The
Aman Ullah et al.
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Catalytic transformation of renewable feedstocks into fine chemicals is in high demands and olefin metathesis is a sophisticated tool for biomass conversion. Nevertheless, the large-scale viability of such processes depends on the conversion efficiency, energy efficiency, catalytic activity, selective conversion
He Nan et al.
Journal of chromatography. A, 1523, 316-320 (2017-06-26)
Silver ion or argentation chromatography utilizes stationary phases containing silver ions for the separation of unsaturated compounds. In this study, a mixed-ligand silver-based ionic liquid (IL) was evaluated for the first time as a gas chromatographic (GC) stationary phase for
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