| Identification | Back Directory | [Name]
SnAP Pip Reagent | [CAS]
1557287-99-6 | [Synonyms]
SnAP Pip Reagent
N1-Boc-N1-[(tributylstannyl)methyl]-1,2-ethanediamine
tert-Butyl (2-aminoethyl)[(tributylstannyl)methyl]carbamate
Carbamic acid, N-(2-aminoethyl)-N-[(tributylstannyl)methyl]-, 1,1-dimethylethyl ester | [Molecular Formula]
C20H44N2O2Sn | [MDL Number]
MFCD28397085 | [MOL File]
1557287-99-6.mol | [Molecular Weight]
463.29 |
| Chemical Properties | Back Directory | [Boiling point ]
458.3±55.0 °C(Predicted) | [density ]
1.108 g/mL | [refractive index ]
n/D1.4860 | [storage temp. ]
-20°C | [form ]
liquid | [pka]
9.42±0.10(Predicted) |
| Hazard Information | Back Directory | [Uses]
SnAP Reagents provide a one-step route, in tandem with various aldehyde substrates, to saturated N-heterocycles. The synthesis of N-heterocycles through SnAP Reagents requires mild reaction conditions, and aldehydes bearing aryl, heteroaryl, glyoxyl, aliphatic, and halogenated groups are well tolerated. This product was introduced in collaboration with the Jeffrey Bode Research Group |
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Sigma-Aldrich
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Synthonix Inc
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