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Merck
CN

304034

2,3-二甲基-2-丁烯 溶液

1.0 M in THF

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线性分子式:
(CH3)2C=C(CH3)2
化学文摘社编号:
分子量:
84.16
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Form:
liquid
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InChI

1S/C6H12/c1-5(2)6(3)4/h1-4H3

SMILES string

C\C(C)=C(\C)C

InChI key

WGLLSSPDPJPLOR-UHFFFAOYSA-N

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

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

用于制备 thexylborane。

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

target_organs

Respiratory system

supp_hazards

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

1.4 °F

flash_point_c

-17 °C

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
Bridgett E Coleman et al.
The journal of physical chemistry. A, 114(48), 12667-12674 (2010-11-17)
The matrix isolation technique, combined with infrared spectroscopy and twin jet codeposition, has been used to characterize intermediates formed during the ozonolysis of 2,3-dimethyl-2-butene (DMB). Absorptions of early intermediates in the twin jet experiments grew up to 200% upon annealing
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

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