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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 Structure](CAS/GIF/142374-19-4.gif) |
| 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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