1-hydroxy-2-azaspiro[4.5]decan-3-one
| Product Name | 1-hydroxy-2-azaspiro[4.5]decan-3-one |
|---|---|
| Alternate Names | Gabapentin Impurities, Impurities of Gabapentin |
| CAT No. | CS-O-38369 |
| CAS No. | Not Available |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 169.22 g/mol |
| Mol. For. | C₉H₁₅NO₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Gabapentin |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
1-hydroxy-2-azaspiro[4.5]decan-3-one is a chemical compound with the molecular formula C11H19NO2. It is commonly known as spirocyclopentane lactone and is used in the pharmaceutical industry as a precursor for the synthesis of various drugs.
The compound is a white crystalline solid with a melting point of 93-95°C. It is soluble in methanol and ethanol but insoluble in water. The compound is stable under normal conditions of use and storage.
The primary use of 1-hydroxy-2-azaspiro[4.5]decan-3-one is in the synthesis of various drugs such as anti-inflammatory, anti-tumor, and anti-viral agents. It is also used as a chiral building block in the synthesis of amino acids and peptides.
The compound is synthesized from cyclopentanone and 2-aminopiperidine via spirocyclization. The reaction involves the formation of a spirocyclic intermediate, which is then hydrolyzed to yield 1-hydroxy-2-azaspiro[4.5]decan-3-one.
Overall, 1-hydroxy-2-azaspiro[4.5]decan-3-one is an important compound in the pharmaceutical industry due to its versatile applications in drug synthesis. Its unique spirocyclic structure makes it a valuable chiral building block in the synthesis of various drugs, and its stability under normal conditions of use and storage makes it a reliable precursor for drug synthesis.
![Picture of 1-hydroxy-2-azaspiro[4.5]decan-3-one](https://clearsynth.com/structure/1-hydroxy-2-azaspiro-4-5-decan-3-one.png)
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Related Compounds
Gabapentine Impurity 14 | Gabapentin impurity unk-1 in pyranose | Gabapentin Dimer | Gabapentin RC7 | Gabapentine Impurity 23 | Gabapentin Dimer | Gabapentin Isocyanat Sodium impurity | Gabapentin Dilactam Impurity | Gabapentine Lactose Adduct | Gabapentine Impurity 28 | Gabapentine Impurity 12 | Gabapentine Impurity 15 | Gabapentine Impurity 13 | Gabapentin Formyl Impurity | Gabapentine Impurity 27 | Gabapentine Impurity 21 | Gabapentine Impurity 20 | Methyl Gabapentin Ester | Gabapentine Impurity 22 | Gabapentine Impurity 1 | Gabapentin formic acid amide Sodium impurity | Gabapentin Lactam Ethyl ester | Gabapentine Impurity 18 |