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Boggle1,3-Diaminopropane
From Wikipedia, the free encyclopedia
| 1,3-Diaminopropane | |
|---|---|
Propane-1,3-diamine | |
other names Trimethylenediamine; TMEDA; propandiamine; 1,3-propylenediamine | |
| Identifiers | |
| CAS number | 109-76-2 |
| PubChem | 428 |
| ChemSpider | 415 |
| SMILES | NCCCN |
| InChI | 1/C3H10N2/c4-2-1-3-5/h1-5H2 |
| InChI key | XFNJVJPLKCPIBV-UHFFFAOYAG |
| Properties | |
| Molecular formula | C3H10N2 |
| Molar mass | 74.12 g mol−1 |
| Hazards | |
| MSDS | External MSDS |
| EU classification | T C |
| (what is this?) (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
1,3-Diaminopropane is a simple amine. The potassium salt is used in the alkyne zipper reaction, first reported by Charles Allen Brown and Ayako Yamashita in 1975.[1]
References
- ^ C. A. Brown and A. Yamashita (1975). [Expression error: Missing operand for > "Saline hydrides and superbases in organic reactions. IX. Acetylene zipper. Exceptionally facile contrathermodynamic multipositional isomeriazation of alkynes with potassium 3-aminopropylamide"]. J. Am. Chem. Soc. 97 (4): 891–892. doi:.
