1,3-Diaminopropane
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| 1,3-Diaminopropane | |
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Propane-1,3-diamine
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Other names
Trimethylenediamine; TMEDA; propandiamine; 1,3-propylenediamine
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| Identifiers | |
| CAS number | 109-76-2  |
| PubChem | 428 |
| ChemSpider | 415 |
| KEGG | C00986 |
| ChEBI | CHEBI:15725 |
| ChEMBL | CHEMBL174324 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C3H10N2 |
| Molar mass | 74.12 g mol−1 |
| Density | 0.880 g/mL |
| Hazards | |
| MSDS | External MSDS |
| EU classification |  T  C |
 (verify) (what is:  / ?)Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| 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]
[edit] References
- ^ C. A. Brown and A. Yamashita (1975). "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:10.1021/ja00837a034.
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