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Wichtige Dokumente
527408
1,3-Hexadien, Mischung aus cis und trans
95%
Synonym(e):
1-Ethyl-1,3-butadiene
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About This Item
Lineare Formel:
C2H5CH=CHCH=CH2
CAS-Nummer:
Molekulargewicht:
82.14
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
95%
Brechungsindex
n20/D 1.438 (lit.)
bp
72-76 °C (lit.)
Dichte
0.714 g/mL at 25 °C (lit.)
SMILES String
CCC=CC=C
InChI
1S/C6H10/c1-3-5-6-4-2/h3,5-6H,1,4H2,2H3
InChIKey
AHAREKHAZNPPMI-UHFFFAOYSA-N
Anwendung
- Ethylene-alt-alpha-Olefin Copolymers by Hydrogenation of Highly Stereoregular cis-1,4 Polydienes: A study on the synthesis and structural characterization of isotactic and syndiotactic polydienes, focusing on copolymers derived from cis-1,4 poly(1,3-hexadiene) (G Ricci et al., 2024).
- Syndiotactic Alternating Ethylene/Propylene Copolymers Obtained Through Non-Catalytic Hydrogenation of Highly Stereoregular cis-1,4 Poly(1,3-diene)s: This article elaborates on the properties of ethylene/propylene copolymers derived from the hydrogenation of 1,3-diene polymers, including 1,3-hexadiene (G Ricci et al., 2017).
- Novel cobalt dichloride complexes with hindered diphenylphosphine ligands: Research on catalytic systems for the polymerization of dienes including 1,3-hexadiene (G Ricci et al., 2019).
- Synthesis and Reactivity of Pyridine (diimine) Molybdenum Olefin Complexes: A detailed look at ethylene dimerization and alkene dehydrogenation processes involving 1,3-hexadiene as an intermediate (MV Joannou et al., 2017).
Zubehör
Produkt-Nr.
Beschreibung
Preisangaben
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
3 - Flammable liquids
WGK
WGK 3
Flammpunkt (°F)
-2.2 °F - closed cup
Flammpunkt (°C)
-19 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Natori et al.
Macromolecules, 31(15), 4687-4694 (1998-07-29)
The n-butyllithium (n-BuLi)/N,N,N',N'-tetramethylethylenediamine (TMEDA) system (with the molar ratio of TMEDA to n-BuLi higher than 4/4) has been found to polymerize 1,3-cyclohexadiene to produce "living" polymer having a narrow molecular weight distribution with well-controlled polymer chain length. The rate of
Laura Torrente-Murciano et al.
Frontiers in chemistry, 2, 37-37 (2014-07-02)
The first example of a tandem reaction involving double-bond migration in combination with telomerization is reported. Homogeneous and heterogeneous Ru catalysts were employed as isomerization catalysts, and telomerization was realized using a homogeneous Pd(0) precursor complex with a N-heterocyclic carbene
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