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1,3-Diaminopropane: Difference between revisions

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Revision as of 14:29, 15 April 2012

1,3-Diaminopropane
Names
IUPAC name Propane-1,3-diamine
Other names Trimethylenediamine; TMEDA; propandiamine; 1,3-propylenediamine
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.367 Edit this at Wikidata
KEGG
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C3H10N2/c4-2-1-3-5/h1-5H2Key: XFNJVJPLKCPIBV-UHFFFAOYSA-N
  • InChI=1/C3H10N2/c4-2-1-3-5/h1-5H2Key: XFNJVJPLKCPIBV-UHFFFAOYAG
SMILES
  • NCCCN
Properties
Chemical formula C3H10N2
Molar mass 74.127 g·mol
Density 0.880 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

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.

References

  1. 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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