74902
1-辛烯
purum, ≥97.0% (GC)
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线性分子式:
CH3(CH2)5CH=CH2
化学文摘社编号:
分子量:
112.21
EC Number:
203-893-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1734497
MDL number:
InChI key
KWKAKUADMBZCLK-UHFFFAOYSA-N
InChI
1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3
SMILES string
CCCCCCC=C
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 %
bp
122-123 °C (lit.)
mp
−101 °C (lit.)
density
0.715 g/mL at 25 °C (lit.)
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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
Mark Kuil et al.
Journal of the American Chemical Society, 128(35), 11344-11345 (2006-08-31)
We report the formation of high-precision catalysts using encapsulated rhodium complexes. In the current example, the encapsulated rhodium catalyst shows unprecedented high selectivity in the rhodium-catalyzed hydroformylation of internal alkenes, forming predominantly one of the branched aldehydes. This catalyst system
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
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
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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