Weight | 120.559 g/mol |
---|---|
Formula | C4H10AlCl |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
Diethylaluminum chloride (96-10-6)
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- Sigma-Aldrich - Diethylaluminum chloride48.40 - 479.00 USD
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- Carbon-13 NMR determination of monomer sequence distribution in ethylene-propylene copolymers prepared with -titanium trichloride-diethylaluminum chloride (Macromolecules, 1982)
- Polymerization of Ethylene with Bis-(cyclopentadienyl)-titanium Dichloride and Diethylaluminum Chloride (Journal of the American Chemical Society, 1960)
- Diethylaluminum chloride complexes of an N-acyloxazolidinone: NMR investigation (Journal of the American Chemical Society, 1993)
- Novel Diethylaluminum Chloride Promoted Reactions of the Azetidine Ring: Efficient and Stereocontrolled Entry to Functionalized Olefins, Pyrrolidines, and Pyrroles (Journal of Organic Chemistry, 1999)
- Stereocontrol by diethylaluminum chloride in the addition of 2-lithiofuran and N-methyl-2-lithioimidazole to -alkoxy nitrones. Total synthesis of 5-O-carbamoylpolyoxamic acid (Tetrahedron Letters, 1993)
- Cyclotrimerization of acetylene by the tris(acetylacetonato)titanium(III)diethylaluminum chloride system (Journal of Polymer Science Part A, 1974)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC[Al](CC)Cl
-
InChIKeyYNLAOSYQHBDIKW-UHFFFAOYSA-M
- Pubchem - Diethylaluminum chloride
- Wikipedia - diethylaluminum chloride
Diethylaluminium chloride is a highly hazardous organic compound and Lewis acid with the chemical formula C4H10AlCl. When dissolved in hexane, diethylaluminum chloride is a colorless liquid. It is used for polyolefin catalysis and as an intermediate in the preparation of organometallic compounds.
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