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Description
- Triallylamine (taa) reacts with primary aromatic amines in the presence of a ruthenium catalyst to form 2-ethyl-3-methylquinolines
- Taa undergoes hydrozirconation followed by transmetalation with germanium tetrachloride to form 1-aza-5-germa-5-chlorobicyclo[3.3.3]undecane. this compound can react with grignard or lithium reagents to form the corresponding 5-organo compounds
- The cycloaddition of taa to fluorinated 1,3,4-oxadiazoles affords octahydro-2,7-methanofuro[3,2-c]pyridines
Specifications
Specifications
| CAS | 102-70-5 |
| Density | 0.79 g/mL (at 25°C (literature)) |
| Boiling Point | 150°C to 151°C (lit.) |
| Molecular Formula | C9H15N |
| Refractive Index | n20/D 1.451 (literature) |
| Linear Formula | (H2C=CHCH2)3 N |
| MDL Number | MFCD00026093 |
| Quantity | 250 mL |
| Synonym | TAA |
| Molecular Weight (g/mol) | 137.22 |
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