Identification | More | [Name]
ISOPROPENYLOXYTRIMETHYLSILANE | [CAS]
1833-53-0 | [Synonyms]
2-(TRIMETHYLSILOXY)PROPENE 2-(TRIMETHYLSILYLOXY)PROPENE ACETONE ENOL TRIMETHYLSILYL ETHER IPOTMS ISOPROPENOXYTRIMETHYLSILANE ISOPROPENYLOXYTRIMETHYLSILANE TRIMETHYLISOPROPENYLOXYSILANE (CH3)3SiOC(CH3)=CH2 Silane, trimethyl[(1-methylethenyl)oxy]- trimethyl[(1-methylethenyl)oxy]-silan trimethyl[(1-methylethenyl)oxy]-Silane trimethyl[(1-methylvinyl)oxy]silane 2-(TRIMETHYLSILYLOXY)PROPENE, 85+% isopropenyloxytrimethylsilane[trimethylsilylatingagent]90+% Isopropenyloxytrimethylsilane(2-Trimethylsiloxypropene) Isopropenyloxytrimethylsilane [Trimethylsilylating Agent] 2-(Trimethylsiloxy)propene, Acetone enol trimethylsilyl ether, IPOTMS Isopropenyl(trimethylsilyl) ether | [EINECS(EC#)]
217-393-1 | [Molecular Formula]
C6H14OSi | [MDL Number]
MFCD00042845 | [Molecular Weight]
130.26 | [MOL File]
1833-53-0.mol |
Safety Data | Back Directory | [Hazard Codes ]
F,Xi | [Risk Statements ]
R11:Highly Flammable. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [RIDADR ]
UN 1993 3/PG 2
| [WGK Germany ]
3
| [F ]
10-21 | [TSCA ]
Yes | [HazardClass ]
3.1 | [PackingGroup ]
II | [HS Code ]
2931900090 |
Hazard Information | Back Directory | [Chemical Properties]
clear colorless liquid | [General Description]
(Isopropenyloxy)trimethylsilane is an enol silyl ether. It participates as nucleophile in Lewis acid-promoted C3-nucleophile substitution of tetracyclic bromide. It is reported to participate in the total synthesis of (±)-powelline. It is reported to participate in dityltin bis(triflate) catalyzed Michael addition reaction of enol silyl ethers. | [Purification Methods]
Purify it by fractional distillation using a very efficient column at atmospheric pressure. It usually contains 5% of hexamethyldisiloxalane which boils at 99-101o, but is generally non-reactive and need not be removed. [Hauser & Hance J Am Chem Soc 71 5091 1952.] It has been distilled under N2 through a 15cm column packed with glass helices. Fraction b 99-104o is further purified by gas chromatography through a Carbowax column (Autoprep A 700) at a column temperature of 87o, and has a retention time of 9.5minutes. [Krüger & Rochow J Organomet Chem 1 476 1963-4.] |
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