| 词条 | 1,1-Dimethylethylenediamine |
| 释义 |
| ImageFile = 1,1-Me2NC2H4NH2.png | ImageSize = | ImageAlt = | IUPACName = N,N-Dimethylethane-1,2-diamine | OtherNames = N,N-Dimethyl-1,2-ethanediamine |Section1={{Chembox Identifiers | CASNo = 108-00-9 | PubChem = 66053 | ChemSpiderID = 59443 | StdInChI = 1S/C4H12N2/c1-6(2)4-3-5/h3-5H2,1-2H3 | StdInChIKey = DILRJUIACXKSQE-UHFFFAOYSA-N | SMILES = CN(C)CCN}} |Section2={{Chembox Properties | C=4|H=12|N=2 | Appearance = Colorless liquid | Density = | MeltingPt = | BoilingPtC = 107 | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }} 1,1-Dimethylethylenediamine is the organic compound with the formula (CH{{sub|3}}){{sub|2}}N)CH{{sub|2}}CH{{sub|2}}NH{{sub|2}}. It is a colorless liquid with a fishy odor. It features one primary amine and a tertiary amine. It is used to prepare a chelating diamine-containing ligands for the preparation of metal catalysts.[1][2] It is a precursor to the drug chloropyramine. See also
References1. ^Chen, Hsuan-Ying; Tang, Hui-Yi; Lin, Chu-Chieh "Ring-Opening Polymerization of Lactides Initiated by Zinc Alkoxides Derived from NNO-Tridentate Ligands" Macromolecules 2006, volume 39, pp. 3745-3752. {{DOI|10.1021/ma060471r}} {{DEFAULTSORT:Dimethylethylenediamine, 1, 2-}}2. ^Tshuva, Edit Y.; Goldberg, Israel; Kol, Moshe; Goldschmidt, Zeev "Zirconium Complexes of Amine-Bis(phenolate) Ligands as Catalysts for 1-Hexene Polymerization: Peripheral Structural Parameters Strongly Affect Reactivity" Organometallics 2001, volume 20, pp. 3017-3028. {{DOI|10.1021/om0101285}} 2 : Diamines|Chelating agents |
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