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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.
2,3,3-Trimethylpentane is a chemical compound in the family of hydrocarbons which has a formula of C 8 H 18. It is an isomer of octane. It has a role as a human metabolite, a bacterial metabolite and a mammalian metabolite. [2] It is an alkane and a volatile organic compound.
Tetramethylbutane, sometimes called hexamethylethane, is a hydrocarbon with formula C 8 H 18 or (H 3 C-) 3 C-C(-CH 3) 3. It is the most heavily branched and most compact of the octane isomers, the only one with a butane (C4) backbone. Because of its highly symmetrical structure, it has a very high melting point and a short liquid range; in fact ...
2,3,4-Trimethylpentane Tetra- tert -butylmethane Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Printable version; In other projects Wikimedia Commons; Wikidata item; Appearance. ... 2,3,4-Trimethylpentane is a branched alkane. It is one of the isomers of octane.
2,2-Dimethylpentane can form a clathrate hydrate with helper gas molecules. The type of clathrate formed is called "clathrate H". 2,2-Dimethylpentane was the first compound for which the structure was determined. The clathrate has 34 molecules of water per molecule, and also has xenon and hydrogen sulfide as helper molecules.
(C 6 H 5) 3 CCl + 2 Na → (C 6 H 5) 3 CNa + NaCl The use of tritylsodium as a strong, non-nucleophilic base has been eclipsed by the popularization of butyllithium and related strong bases. The unmodified anion is red, and can be used as an indicator in acid–base titrations .
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]