| Weight | 212.296 g/mol |
|---|---|
| Formula | C14H16N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
1,2-diphenylethane-1,2-diamine (5700-60-7)
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- Asymmetric organocatalysis of the addition of acetone to 2-nitrostyrene using N-diphenylphosphinyl-1,2-diphenylethane-1,2-diamine (PODPEN) (Tetrahedron Letters, 2010)
- Simple chiral derivatisation protocols for NMR analysis of the enantiopurity of 1,2-diphenylethane-1,2-diamine and N-Boc-cyclohexane-1,2-diamine (Tetrahedron-asymmetry, 2008)
- Application of proline-functionalised 1,2-diphenylethane-1,2-diamine (DPEN) in asymmetric transfer hydrogenation of ketones (European Journal of Organic Chemistry, 2011)
- Polystyrene copolymer supported by substituted (1R,2R)-1, 2-diphenylethane-1,2-diamine-copper(II) complexes: a recyclable catalyst for asymmetric Henry reactions (Tetrahedron-asymmetry, 2014)
- 1,2-Diphenylethane-1,2-diamine: an effective NMR chiral solvating agent for chiral carboxylic acids (Journal of The Chemical Society-perkin Transactions 1, 1994)
- Synthesis, structural and optical properties of novel 3-(3,5-dimethyl-1H-pyrazol-1-yl)-1-(diphenylphosphino)-2-((diphenylphosphino)methyl)-3-methylbutanone-1,2-diphenylethane-1,2-diamine tungsten dicarbonyl (PyrPMB-W) nanostructure thin film (Optical Materials, 2015)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(C(C2=CC=CC=C2)N)N
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InChIKeyPONXTPCRRASWKW-UHFFFAOYSA-N
- Pubchem - 1,2-diphenylethane-1,2-diamine
- Wikipedia - Diphenylethylenediamine
1,2-Diphenyl-1,2-ethylenediamine is an organic compound with the formula H2NCHPhCHPhNH2, where Ph is C6H5, phenyl. This diamine is a precursor to a ligand for certain homogeneous hydrogenation catalysts. It can be prepared from benzil by reductive amination.
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