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{{Chembox |
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{{Chembox |
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| verifiedrevid = 441102222 |
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|verifiedrevid = 442266594 |
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| ImageFile = Tris(dimethylamino)aluminium dimer.png |
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|ImageFile = Tris(dimethylamino)aluminium dimer.png |
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|IUPACName = <em>N</em>--<em>N</em>-methylmethanamine |
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| ImageSize = |
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|Section1={{Chembox Identifiers |
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| ImageAlt = |
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|CASNo_Ref = {{cascite|correct|??}} |
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| IUPACName = |
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|CASNo = 32093-39-3 |
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| OtherNames = |
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|ChemSpiderID = 21170557 |
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| Section1 = {{Chembox Identifiers |
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| CASNo = 32093-39-3 |
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|EC_number = 626-275-2 |
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|DTXSID = DTXSID60586931 |
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| PubChem = |
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|InChI = InChI=1S/6C2H6N.2Al/c6*1-3-2;;/h6*1-2H3;;/q6*-1;2*+3 |
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| SMILES = }} |
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|InChIKey = JGZUJELGSMSOID-UHFFFAOYSA-N |
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| Section2 = {{Chembox Properties |
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|PubChem = 16688802 |
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| C = 12 | H = 36 | Al = 2 | N = 6 |
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|SMILES = CN(C)(N(C)C)N(C)C.CN(C)(N(C)C)N(C)C}} |
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| MolarMass = |
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|Section2={{Chembox Properties |
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| Appearance = Colorless solid |
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|C=12 | H=36 | Al=2 | N=6 |
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| Density = |
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|Appearance = Colorless solid |
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| MeltingPt = |
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|Density = 0.865 g/cm<sup>3</sup> |
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| BoilingPt = |
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|MeltingPt = 82-84 °C |
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| Solubility = }} |
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|BoilingPt = 90 °C |
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| Section3 = {{Chembox Hazards |
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| MainHazards = |
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| FlashPt = |
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| Autoignition = }} |
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|Section3={{Chembox Hazards |
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'''Tris(dimethylamino)aluminium dimer''', formally bis(μ-dimethylamino)tetrakis(dimethylamino)dialuminium, is an ] of ]. This compound may be used as a precursor to other aluminium complexes. |
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|Hazards_ref =<ref>{{cite web|title =Tris(dimethylamido)aluminum(III)|url=https://www.americanelements.com/tris-dimethylamido-aluminum-iii-32093-39-3|publisher = ]|accessdate = August 21, 2019}}</ref> |
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|GHSPictograms = {{GHS02}}{{GHS05}} |
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|GHSSignalWord = Danger |
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|HPhrases = {{H-phrases|260|314}} |
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|PPhrases = {{P-phrases|223|231+232|260|264|280|301+330+331|303+361+353|304+340|305+351+338|310|321|335+334|363|370+378|402+404|405|501}} |
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|MainHazards = Flammable, Corrosive |
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|FlashPt = 21.1 °C}} |
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}} |
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'''Tris(dimethylamino)aluminium dimer''', formally bis(μ-dimethylamino)tetrakis(dimethylamino)dialuminium, is an ] of ]. This compound may be used as a precursor to other aluminium complexes. |
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Commercially available, this compound may be prepared from lithium dimethylamide and ].<ref> {{Cite journal | doi = 10.1016/S0277-5387(00)80578-1 | title = Structural and spectroscopic characterization of the compounds 2, 2, 2 (1-Ad = 1-adamantanyl) and | year = 1990 | last1 = Waggoner | first1 = K.M. | last2 = Olmstead | first2 = M.M. | last3 = Power | first3 = P.P. | journal = Polyhedron | volume = 9 | issue = 2–3 | pages = 257–263}}</ref> |
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Commercially available, this compound may be prepared from lithium dimethylamide and ].<ref>{{Cite journal | doi = 10.1016/S0277-5387(00)80578-1 | title = Structural and spectroscopic characterization of the compounds 2, 2, 2 (1-Ad = 1-adamantanyl) and | year = 1990 | last1 = Waggoner | first1 = K.M. | last2 = Olmstead | first2 = M.M. | last3 = Power | first3 = P.P. | journal = Polyhedron | volume = 9 | issue = 2–3 | pages = 257–263}}</ref> |
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==References== |
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==References== |
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{{Reflist}} |
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<references/> |
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{{organic-chem-stub}} |
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] |
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] |
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