| Weight | 153.269 g/mol |
|---|---|
| Formula | C10H19N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2-Azaspiro[5.5]undecane (180-48-3)
180-48-3
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- Sigma-Aldrich - Search for 2-Azaspiro[5.5]undecane
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- A stereoselective approach to the azaspiro[5.5]undecane ring system using a conjugate addition/dipolar cycloaddition cascade: application to the total synthesis of (+/-)-2,7,8-epi-perhydrohistrionicotoxin. (Journal of Organic Chemistry, 2008)
- Tricarbonylcyclohexadienyliumiron Complexes in the Synthesis of 2-Azaspiro[5.5]undecane System with Tunable Amide. (Journal of Organic Chemistry, 1996)
- Formal Synthesis of a 2- and 8-Functionalized 1,4,7-Trioxa-10-azaspiro[5.5]undecane (Synthesis, 1995)
- Synthesis and biochemical studies of spirocyclic amino acids. II. Activity of 2-azaspiro[5.5]undecane-7-carboxylates as GABA-uptake inhibitors (European Journal of Medicinal Chemistry, 1995)
- Synthesis of dipeptides from N-hydroxy-3-azaspiro[5,5]undecane-2,4-dione activated -amino acids (Tetrahedron-asymmetry, 2011)
- Simple, Improved Synthesis of 3-Azaspiro[5,5]undecane-2,4-dione, the Precursor of Gabapentin (Organic Preparations and Procedures International, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 180-48-3
-
SMILESC1CCC2(CC1)CCCNC2
-
InChIKeyVZUJZECRVUMMJI-UHFFFAOYSA-N
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Most-cited Publications
Safety
Alternate Names
Estimated Properties
| Boiling Point | 223.66 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 228.14 C | EPI Suite |
| Density | 0.91 g/cm3 | EPA T.E.S.T. |
| Flash Point | 80.56 C | EPA T.E.S.T. |
| Melting Point | 39.95 C | EPI Suite |
| Water Solubility | 3545.26 mg/L | EPA T.E.S.T. |
| Water Solubility | 10364 mg/L | EPI Suite |
External Links
Synthesis
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