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2,3-Dimethyl-2-buten -Lösung
1.0 M in THF
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About This Item
Lineare Formel:
(CH3)2C=C(CH3)2
CAS-Nummer:
Molekulargewicht:
84.16
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
Empfohlene Produkte
Form
liquid
Selbstzündungstemp.
754 °F
Konzentration
1.0 M in THF
Dichte
0.857 g/mL at 25 °C
Lagertemp.
2-8°C
SMILES String
C\C(C)=C(\C)C
InChI
1S/C6H12/c1-5(2)6(3)4/h1-4H3
InChIKey
WGLLSSPDPJPLOR-UHFFFAOYSA-N
Allgemeine Beschreibung
2,3-Dimethyl-2-butene undergoes ozonolysis in dark to yield hydroxyl radical. Reaction of ozone with 2,3-dimethyl 2-butene was investigated using a flow-tube interfaced to UV photoelectron spectrometer. It forms adduct with thianthrene cation radical tetrafluoroborate at 0°C and -15°C.
Anwendung
Used for the preparation of thexylborane.
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
Zielorgane
Respiratory system
Zusätzliche Gefahrenhinweise
Lagerklassenschlüssel
3 - Flammable liquids
WGK
WGK 3
Flammpunkt (°F)
1.4 °F
Flammpunkt (°C)
-17 °C
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Bing-Jun Zhao et al.
The Journal of organic chemistry, 71(10), 3737-3742 (2006-05-06)
Thianthrene cation radical tetrafluoroborate (Th*+ BF4-) has been found to add to 2,3-dimethyl-2-butene (DMB) at 0 degrees C and -15 degrees C. The adduct, 2,3-dimethyl-2,3-(5,10-thianthreniumdiyl)butane ditetrafluoroborate (12), was isolated at -15 degrees C, and its 1H NMR spectrum was recorded
Maryline Pflieger et al.
Environmental science & technology, 47(12), 6239-6246 (2013-05-15)
In order to investigate the heterogeneous oxidation kinetics of the herbicide terbuthylazine (TERB), a stable and reproducible generation system of "dark" hydroxyl radical in the gas phase was developed and optimized using a PTR-MS. TERB was adsorbed on silica particles
P Di Mascio et al.
Free radical biology & medicine, 12(6), 471-478 (1992-01-01)
Ultraweak chemiluminescence arising from lipoperoxidation has been attributed by several authors to the radiative deactivation of singlet oxygen and triplet carbonyl products. The latter emitters have been suggested to come from annihilation of RO. and ROO. radicals as well as
Bert F Sels et al.
Journal of the American Chemical Society, 129(21), 6916-6926 (2007-05-10)
A heterogeneous catalyst containing MoO42- exchanged on layered double hydroxides (Mo-LDHs) is used to produce 1O2 from H2O2, and with this dark 1O2, unsaturated hydrocarbons are oxidized in allylic peroxides. The oxidation kinetics are studied in detail and are compared
Relative reactivities of the excited states of furocoumarins for [2 + 2] photocycloaddition reaction with tetramethylethylene.
S C Shim et al.
Photochemistry and photobiology, 45(4), 453-458 (1987-04-01)
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