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About This Item
Linear Formula:
(CH3)2C=C(CH3)2
CAS Number:
Molecular Weight:
84.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
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
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
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
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)
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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