| Identification | More | [Name]
1,2-BIS(TRIMETHYLSILYLOXY)CYCLOBUTENE | [CAS]
17082-61-0 | [Synonyms]
1,2-BIS(TRIMETHYLSILOXY)CYCLOBUTENE
1,2-BIS(TRIMETHYLSILYLOXY)CYCLOBUTENE
BIS(TRIMETHYLSILOXY)CYCLOBUTENE
1,2-BIS(TRIMETHYLSILYLOXY)CYCLOBUTENE, 9 5+%
1,2-Bis(trimethylsiloxy)cyclobutenepurum
95+%(gc)
1,2-BIS(TRIMETHYLSILOXY)CYCLOBUTENE PURUM 95+ % (GC)
BIS(TRIMETHYLSILOXY)CYCLOBUTENE ,95%
[1-Cyclobutene-1,2-diylbis(oxy)]bis[trimethylsilane]
1,2-Bis(trimethylsiloxy)-1-cyclobutene | [Molecular Formula]
C10H22O2Si2 | [MDL Number]
MFCD00010798 | [Molecular Weight]
230.45 | [MOL File]
17082-61-0.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless liquid | [Boiling point ]
58-59 °C2 mm Hg(lit.) | [density ]
0.897 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.435(lit.)
| [Fp ]
142 °F
| [storage temp. ]
2-8°C
| [solubility ]
sol hydrocarbons and ethers. | [form ]
clear liquid | [color ]
Colorless to Light yellow | [Specific Gravity]
0.87 | [Hydrolytic Sensitivity]
7: reacts slowly with moisture/water | [BRN ]
1367530 | [InChIKey]
WOBRFSDEZREQAB-UHFFFAOYSA-N | [CAS DataBase Reference]
17082-61-0(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
1993 | [WGK Germany ]
3
| [F ]
10-21 | [TSCA ]
No | [HS Code ]
2931.90.6000 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless liquid | [Uses]
1,2-Bis(trimethylsilyloxy)cyclobutene is a useful chemical reactant used in the preparation and biological activity of serine and threonine β-lactones as inhibitors of hepatitis A virus 3C cysteine proteinase. | [Application]
Used as a suitable reagent for annulation processes and 4-keto ester synthesis. | [General Description]
Photocycloaddition of 2-cyclohexenones to 1,2-bis(trimethyl-siloxy)cyclobutene has been studied. It undergoes Aldol condensation reaction with carbonyl compounds. It reacts with Br2 to give cyclobutanedione. | [Synthesis]
1,2-Bis(trimethylsilyloxy)cyclobutene is prepared as a colorless liquid by acyloin condensation of Diethyl Succinate
(dispersed Na in toluene or Et2O, reflux) using Chlorotrimethylsilane as trapping agent. | [storage]
Use in a fume hood; the compound is stable for years if stored in a
tightly screw-capped bottle. Prolonged exposure to moist air leads to decomposition. |
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