O2501
1,7-Octadiene
98%
Sinonimo/i:
α,ψ-Octadiene
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100 G
76,40 €
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Cambia visualizzazione
100 G
76,40 €
About This Item
Formula condensata:
CH2=CH(CH2)4CH=CH2
Numero CAS:
Peso molecolare:
110.20
Beilstein:
605288
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
98%
Indice di rifrazione
n20/D 1.422 (lit.)
P. ebollizione
114-121 °C (lit.)
Densità
0.746 g/mL at 25 °C (lit.)
Stringa SMILE
C=CCCCCC=C
InChI
1S/C8H14/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-8H2
XWJBRBSPAODJER-UHFFFAOYSA-N
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Descrizione generale
1,7-Octadiene can serve as a crosslinker and source of ethylene for a variant of Mori′s conditions in CEYM-related reactions. [1]
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
50.0 °F - closed cup
Punto d’infiammabilità (°C)
10 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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The role surface capping molecules play in dictating the optical properties of semiconductor nanocrystals (NCs) is becoming increasingly evident. In this paper the role of surface capping molecule polarity on the optical properties of germanium NCs (Ge NCs) is explored.
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Nanoscale, 10(39), 18706-18719 (2018-10-03)
This study reports the preparation of functional bioinorganic hybrids, through application of the thiol-ene reaction, that exhibit catalytic activity and photoluminescent properties from enzymes and freestanding silicon nanocrystals. Thermal hydrosilylation of 1,7-octadiene and alkene-terminated poly(ethylene oxide)methyl ether with hydride-terminated silicon
Ian W Ashworth et al.
Chemical communications (Cambridge, England), 46(38), 7145-7147 (2010-09-08)
In the RCM reactions of a series of simple α,ω-dienes, the relative order of reactivity has been unambiguously determined showing that cyclohexene forms faster than cyclopentene or cycloheptene. 1,5-Hexadiene inhibits the RCM of 1,7-octadiene; 1,5-hexadiene cannot progress to the RCM
Santos Fustero et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(35), 10991-10997 (2012-08-02)
The use of 1,7-octadiene as an in situ source of ethylene led us to develop a novel multicomponent tandem cross-enyne metathesis (CEYM)-Diels-Alder reaction. The process can be considered a relay metathesis, in which the ethylene liberated in the ring-closing metathesis
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