Determine the necessary mass, volume, or concentration for preparing a solution.
0.5M in toluene for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Tebbe reagent is a Lewis acid stabilized organometallic compound, which is used to transform carbonyl groups into β-substituted methylenes. It also reacts with a wide range of carbonyl compounds, including esters, amides, and lactones to yield corresponding olefins.Tebbe reagent can be used:For the conversion of carbonyl groups of chlorophyll derivatives into the corresponding exo-methylene (or vinylidene) groups.In the synthesis of β-C-glycosides from 3-OH glycol esters.As a versatile methylenation reagent for the conversion of ketones and aldehydes to olefins. It offers facile reaction with hindered ketones and allows the conversion of esters to vinyl ethers.To olefinate aldehydes.To methylenate a chiral polyhydroxyketone with high diasteroselctivity.
| Canonical Smiles | [CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2.C[Al](C)C[Ti]Cl |
|---|---|
| InChIKey | QEJAQNUJXFLWSP-UHFFFAOYSA-M |
| INCHI | 1S/2C5H5.2CH3.CH2.Al.ClH.Ti/c2*1-2-4-5-3-1;;;;;;/h2*1-5H;2*1H3;1H2;;1H;/q;;;;;;;+1/p-1 |
| UN Number | 2924 |
| Molecular Weight | 284.58 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| Flash Point(°F) | 39.2 °F - closed cup |
|---|---|
| Flash Point(°C) | 4 °C - closed cup |