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Sigma Aldrich 1,2-Diaminocyclohexane, mixture of cis and trans
Description
- 1,2-diaminocyclohexane undergoes non-templated reaction with homochiral as well as the racemic form of trans-1,2-diaminocyclohexane with terephthaldehyde to yield (3+3)-cyclocondensed molecular triangles
- It acts as ligand and forms organotin complexes, having potential applications as metal-based antitumour drugs.1,2-diaminocyclohexane was used in the synthesis of chiral ruthenium(iv)-oxo complexes
Specifications
Specifications
| CAS | 694-83-7 |
| Density | 0.931 g/mL (at 25°C (literature)) |
| Boiling Point | 92°C to 93°C (18 mmHg) |
| Molecular Formula | C6H14N2 |
| Refractive Index | n20/D 1.49 (literature) |
| Linear Formula | C6H10(NH2)2 |
| MDL Number | MFCD00001491 |
| Quantity | 18 L |
| Synonym | 1,2-Cyclohexanediamine; DHC 99 |
| Molecular Weight (g/mol) | 114.19 |
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