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Key Documents

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O2501

Sigma-Aldrich

1,7-Octadiene

98%

Sinónimos:

α,ψ-Octadiene

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About This Item

Fórmula lineal:
CH2=CH(CH2)4CH=CH2
Número de CAS:
3710-30-3
Peso molecular:
110.20
Beilstein/REAXYS Number:
605288
EC Number:
223-054-9
MDL number:
MFCD00008668
UNSPSC Code:
12352100
PubChem Substance ID:
24897962
NACRES:
NA.22

Quality Level

100

assay

98%

refractive index

n20/D 1.422 (lit.)

bp

114-121 °C (lit.)

density

0.746 g/mL at 25 °C (lit.)

SMILES string

C=CCCCCC=C

InChI

1S/C8H14/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-8H2

Inchi Key

XWJBRBSPAODJER-UHFFFAOYSA-N

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General description

1,7-Octadiene can serve as a crosslinker and source of ethylene for a variant of Mori′s conditions in CEYM-related reactions.

Application

1,7-Octadiene has been used in a study to assess the structure and reaction rate in olefin ring-closing metathesis of a series of simple dienes. It has also been used in a study to investigate micropatterned surfaces prepared by plasma polymerization.

pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

50.0 °F - closed cup

flash_point_c

10 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
BCCK8079
STBL3256
STBL1570
STBK7985
STBK3439

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Sigma-Aldrich

295035

1,3-Butadiene

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
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
Christopher Jay T Robidillo et al.
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
E Filová et al.
Physiological research, 58(5), 669-684 (2008-12-20)
Micropatterned surfaces have been used as a tool for controlling the extent and strength of cell adhesion, the direction of cell growth and the spatial distribution of cells. In this study, chemically micropatterned surfaces were prepared by successive plasma polymerization
Rahul M Visalakshan et al.
ACS applied materials & interfaces, 11(31), 27615-27623 (2019-07-17)
The nature of the protein corona forming on biomaterial surfaces can affect the performance of implanted devices. This study investigated the role of surface chemistry and wettability on human serum-derived protein corona formation on biomaterial surfaces and the subsequent effects
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