304034
2,3-Dimethyl-2-butene solution
1.0 M in THF
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About This Item
Fórmula lineal:
(CH3)2C=C(CH3)2
Número de CAS:
Peso molecular:
84.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Productos recomendados
form
liquid
autoignition temp.
754 °F
concentration
1.0 M in THF
density
0.857 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
C\C(C)=C(\C)C
InChI
1S/C6H12/c1-5(2)6(3)4/h1-4H3
InChI key
WGLLSSPDPJPLOR-UHFFFAOYSA-N
General description
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.
Application
Used for the preparation of thexylborane.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
supp_hazards
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
1.4 °F
flash_point_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
N Haga et al.
Photochemistry and photobiology, 61(6), 557-562 (1995-06-01)
The mechanism of photocycloaddition of 2'-deoxyuridine (1a) and thymidine (1b) to 2,3-dimethyl-2-butene (Bu) in acetonitrile by UV irradiation has been studied. The reciprocal quantum yield for the cycloaddition increased linearly with reciprocal concentrations of Bu in acetonitrile to give limiting
L R Pohl et al.
Biochemical and biophysical research communications, 117(2), 367-371 (1983-12-16)
Although indirect evidence has suggested that liver microsomal cytochrome P-450 can reductively dehalogenate several compounds to carbene metabolites, there has been no direct proof for the formation of these reactive species. We report in this paper that carbenes can be
Andrew T Lambe et al.
Environmental science & technology, 41(7), 2357-2363 (2007-04-19)
We present a novel method for continuous, stable OH radical production for use in smog chamber studies, especially those focused on organic aerosol aging. Our source produces OH radicals from the reaction of 2,3-dimethyl-2-butene and ozone and is unique as
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