Tetramethylethylene, 97%
Tetramethylethylene, 97%
Tetramethylethylene, 97%
Thermo Scientific Chemicals

Tetramethylethylene, 97%

CAS: 563-79-1 | C6H12 | 84.162 g/mol
製品番号(カタログ番号) A13201.14
または、製品番号A13201-14
価格(JPY)
-
数量:
25 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS563-79-1
IUPAC Name2,3-dimethylbut-2-ene
Molecular FormulaC6H12
InChI KeyWGLLSSPDPJPLOR-UHFFFAOYSA-N
SMILESCC(C)=C(C)C
さらに表示
FormLiquid
Appearance (Color)Clear colorless
Refractive Index1.4100-1.4150 @ 20?C (UK sourced material only)
Assay (GC)≥96.0%
Tetramethylethylene is an pharmaceutical intermediate. Ozonolysys in neat tetramethyleneethylene gives tetramethyleneethylene epoxide as product.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Tetramethylethylene is an pharmaceutical intermediate. Ozonolysys in neat tetramethyleneethylene gives tetramethyleneethylene epoxide as product.

Solubility
Soluble in water (0.071 g/L)

Notes
Store at room temperature. Incompatible with oxidizing agents. Air sensitive.
RUO – Research Use Only

General References:

  1. H. Niki.; P. D. Maker.; C. M. Savage.; L. P. Breitenbach.; M. D. Hurley. FTIR spectroscopic study of the mechanism for the gas-phase reaction between ozone and tetramethylethylene. J. Phys. Chem. 1987, 91 (4),941-946 .
  2. Linus Pauling.; L. O. Brockway. Carbon—Carbon Bond Distances. The Electron Diffraction Investigation of Ethane, Propane, Isobutane, Neopentane, Cyclopropane, Cyclopentane, Cyclohexane, Allene, Ethylene, Isobutene, Tetramethylethylene, Mesitylene, and Hexamethylbenzene. Revised Values of Covalent Radii. J. Am. Chem. Soc. 1937, 59 (7),1223-1236 .
  3. Precursor of the sterically hindered hydroborating reagent, thexylborane, introduced by Brown: J. Am. Chem. Soc., 94, 3561 (1972). For review of its chemistry, see: Synthesis, 77 (1974). This reagent should be freshly prepared since it rearranges on standing to 2,3-dimethyl-1-butylborane.