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It has the chemical formula (CH 3) 2 CHCH(CH 3) 2. It is a colorless liquid which boils at 57.9 °C. It is a colorless liquid which boils at 57.9 °C. References
Dimethylbutadiene, formally referred to as 2,3-dimethyl-1,3-butadiene, is an organic compound with the formula (CH 3) 2 C 4 H 4. It is colorless liquid which served an important role in the early history of synthetic rubber. It is now a specialty reagent.
The molecular formula C 6 H 14 (molar mass: 86.17 g/mol) may refer to: Dimethylbutanes 2,2-Dimethylbutane; 2,3-Dimethylbutane; Hexane; Methylpentanes 2-Methylpentane;
2,3-Dimethyl-1-butene is an organic compound with the formula CH 2 =C(CH 3)CH(CH 3) 2. Like the other isomers of dimethylbutene, it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene. It is a precursor to the commercial fragrance tonalide. [1]
The boiling point of 89.7 °C is 0.3 °C higher than the value of 89.4 °C predicted by Wiener's formula, based on the structure of the molecule and the boiling point of n-heptane. [ 2 ] [ 3 ] The speed of sound at 3 MHz is 1149.5 m/s at 20 °C and 889.5 m/s at 80 °C.
Dimethylbutene is an alkene with a molecular formula C 6 H 12. It has the following possible structural isomers: 2,3-Dimethyl-1-butene; 3,3-Dimethyl-1-butene;
Triptane, or 2,2,3-trimethylbutane, is an organic chemical compound with the molecular formula C 7 H 16 or (H 3 C-) 3 C-C(-CH 3) 2 H. It is therefore an alkane, specifically the most compact and heavily branched of the heptane isomers, the only one with a butane (C 4) backbone.
[2] [5] The compound is used as a reactant in the synthesis of a number of compounds. Notably it is used to synthesize 2,3-dimethylbut-2-ene, and is then converted to 2,3-dimethylbutane-2,3-diol and methyl tert-butyl ketone, better known as pinacolone. Pinacolone itself is then used in synthesis for number of pesticides.