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About This Item
Linear Formula:
CH3(CH2)5CH=CH2
CAS Number:
Molecular Weight:
112.21
Beilstein:
1734497
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
vapor density
3.9 (vs air)
vapor pressure
36 mmHg ( 38 °C)
grade
purum
Assay
≥97.0% (GC)
form
liquid
autoignition temp.
446 °F
expl. lim.
3.9 %
refractive index
n20/D 1.408 (lit.)
n20/D 1.409 (lit.)
n20/D 1.409
bp
122-123 °C (lit.)
mp
−101 °C (lit.)
density
0.715 g/mL at 25 °C (lit.)
SMILES string
CCCCCCC=C
InChI
1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3
InChI key
KWKAKUADMBZCLK-UHFFFAOYSA-N
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I N White et al.
Biochemical pharmacology, 35(9), 1569-1575 (1986-05-01)
The enzymic activation of a model olefin oct-1-ene was studied in rat liver microsomal systems in vitro. An active metabolite was trapped using N-acetylcysteine and identified by means of capillary GLC/mass spectrometry and 360 MHz 1H NMR as S-3-oxo-octyl-N-acetylcysteine. A
Sara M Aschmann et al.
Environmental science & technology, 44(10), 3825-3831 (2010-04-28)
Products of the gas-phase reactions of OH radicals with 1-octene and 7-tetradecene have been investigated at 296 +/- 2 K and atmospheric pressure of air, using gas chromatography, direct air sampling atmospheric pressure ionization tandem mass spectrometry, and in situ
F P Guengerich
Biochemical and biophysical research communications, 138(1), 193-198 (1986-07-16)
The heme in rat liver microsomal cytochrome P-450 was labeled with 14C or 3H and the microsomes were fractionated after in vitro incubations with a variety of agents known to destroy cytochrome P-450 heme. A major fraction of the heme
Frans T I Marx et al.
Journal of molecular modeling, 15(11), 1371-1381 (2009-06-02)
The productive self-metathesis reaction of 1-octene in the presence of the Phobcat precatalyst [RuCl(2)(Phoban-Cy)(2)(=CHPh)] using density functional theory was investigated and compared to the Grubbs 1 precatalyst [RuCl(2)(PCy(3))(2)(=CHPh)]. At the GGA-PW91/DNP level, the geometry optimization of all the participating species
Photoactivated DNA cleavage by compounds structurally related to the bithiazole moiety of bleomycin.
J C Quada et al.
Bioorganic & medicinal chemistry, 9(9), 2303-2314 (2001-09-13)
The syntheses of several novel halogenated bithiazoles structurally related to the bithiazole moiety of bleomycin A(5) are described. Also described is the ability of these compounds to mediate photoactivated DNA cleavage. Chlorinated bithiazole analogues were shown to be much more
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