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| | N-BOC-4-PIPERIDINEACETALDEHYDE Basic information |
| Product Name: | N-BOC-4-PIPERIDINEACETALDEHYDE | | Synonyms: | 1-(tert-butyloxycarbonyl)-piperidine-4-acetaldehyde;tert-Butyl 4-(formylmethyl)piperidine-1-carboxylate;tert-Butyl 4-(2-oxoethyl);n-boc-4-piperidineacetaldehyde;1-PIPERIDINE CARBOXYLIC ACID, 4-(2-OXOETHYL)-1,1-D;1-Boc-4-(2-oxo-ethyl)piperidine;tert-butyl 4-(2-oxoethyl)piperidin-1-carboxylate;1-Piperidinecarboxylic acid, 4-(2-oxoethyl)-, 1,1-diMethylethyl ester | | CAS: | 142374-19-4 | | MF: | C12H21NO3 | | MW: | 227.3 | | EINECS: | | | Product Categories: | pharmacetical | | Mol File: | 142374-19-4.mol |  |
| | N-BOC-4-PIPERIDINEACETALDEHYDE Chemical Properties |
| Melting point | 38-42 °C | | Boiling point | 318.1±15.0 °C(Predicted) | | density | 1.035±0.06 g/cm3(Predicted) | | Fp | >110℃ | | storage temp. | Inert atmosphere,Store in freezer, under -20°C | | pka | -1.62±0.40(Predicted) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26 | | WGK Germany | 3 |
| | N-BOC-4-PIPERIDINEACETALDEHYDE Usage And Synthesis |
| Uses | Reactant for synthesis of:
- Pim-1 inhibitors
- Selective GPR119 agonists for type II diabetes
Reactant for:
- α-arylation of aldehydes
- Enantioselective α-benzylation of aldehydes via photoredox organocatalysis
- Enantioselective α?triflouromethylation of aldehydes
| | Uses | N-Boc-4-piperidineacetaldehyde is used in the preparation of benzofuran-2-carboxylic acid based Pim-1 inhibitors. |
| | N-BOC-4-PIPERIDINEACETALDEHYDE Preparation Products And Raw materials |
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