129259
2,3-Dimethyl-2-butene
98%
Synonym(s):
Tetramethylethylene
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About This Item
Linear Formula:
(CH3)2C=C(CH3)2
CAS Number:
Molecular Weight:
84.16
Beilstein:
1361357
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Recommended Products
vapor pressure
215 mmHg ( 37.7 °C)
Assay
98%
form
liquid
autoignition temp.
754 °F
refractive index
n20/D 1.412 (lit.)
bp
73 °C (lit.)
mp
−75 °C (lit.)
density
0.708 g/mL at 25 °C (lit.)
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
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
17.6 °F - closed cup
Flash Point(C)
-8 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The hydroboration of alkenes of diverse structural types by assorted N-heterocyclic carbene boranes can be accomplished by addition of 5-10% diiodine. For example, reaction of 1,3-dimethylimidazol-2-ylidene borane (diMe-Imd-BH3) with 10% I2 followed by addition of 2,3-dimethyl-2-butene provided the corresponding thexyl
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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
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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
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.
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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
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