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128554

Sigma-Aldrich

1,5-Hexadiene

97%

Sinónimos:

Biallyl, Diallyl

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About This Item

Fórmula lineal:
H2C=CHCH2CH2CH=CH2
Número de CAS:
592-42-7
Peso molecular:
82.14
Beilstein/REAXYS Number:
1731106
EC Number:
209-754-7
MDL number:
MFCD00008666
UNSPSC Code:
12352100
PubChem Substance ID:
24847866
NACRES:
NA.22

vapor pressure

367 mmHg ( 37.7 °C)

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.)

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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Application

1,5-Hexadiene was used to study the Pd(II)-catalyzed cycloisomerization of functionalized 1,5-hexadienes.

For use with

Referencia del producto
Descripción
Precios

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

-16.6 °F - closed cup

flash_point_c

-27 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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.
ChemSusChem, 10(10), 2167-2174 (2017-03-02)
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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