Introduction:Basic information about 1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE CAS 128244-01-9, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Basic information
| Product Name: | 1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE |
| Synonyms: | 1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE;1,7-Diazaspiro[4.4]nonane, 1-(phenylMethyl)-;1-Benzyl-1,7-diazaspiro[4.4]nonane heMioxalte;1-Benzyl-1,7-diazaspiro[4.4]nonane hemioxalate, 95% |
| CAS: | 128244-01-9 |
| MF: | C14H20N2 |
| MW: | 216.32 |
| EINECS: | |
| Product Categories: | |
| Mol File: | 128244-01-9.mol |
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1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Chemical Properties
| Boiling point | 328.1±17.0 °C(Predicted) |
| density | 1.08±0.1 g/cm3(Predicted) |
| storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C |
| pka | 10.68±0.20(Predicted) |
Safety Information
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36 |
| HS Code | 29339900 |
1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Usage And Synthesis
| Synthesis | The synthesis of the 1-benzyl-1,7-diazaspiro[4,4]nonane core structure (a spirocyclic diamine structure) typically involves a multi-step reaction to construct two fused pyrrolidine rings sharing a single spirocyclic carbon atom. A common approach is to utilize suitable linear or pre-cyclized precursors for reductive amination or cyclization. For example, the synthesis can begin with a protected diamine derivative followed by a key step, such as an intramolecular cyclization of a linear intermediate containing a primary amine and an electrophilic center (e.g., a toluenesulfonate or halide), to form one of the pyrrolidine rings. The second ring forms the spirocyclic center, typically constructed via a subsequent cyclization reaction or a [3+2] cycloaddition reaction. The final step is the introduction of a benzyl group, usually through N-alkylation of the secondary amine with benzyl bromide or benzyl chloride, or reductive amination with benzaldehyde, followed by removal of the remaining protecting group to yield 1-benzyl-1,7-diazaspiro[4.4]nonane. |
1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Preparation Products And Raw materials