| Name： | N-BOC-4-PIPERIDINEACETALDEHYDE |
| CAS： | 142374-19-4 |
| Synonyms： | 1-PIPERIDINECARBOXYLIC ACID, 4-(2-OXOETHYL)-, 1,1-DIMETHYLETHYL ESTER ; N-BOC-4-PIPERIDINEACETALDEHYDE ; 1-BOC-4-(2-OXO-ETHYL)PIPERIDINE ; N-BOC-PIPERIDINYL-4-ACETALDEHYDE ; TERT-BUTYL 4-(FORMYLMETHYL)PIPERIDINE-1-CARBOXYLATE ; 2-(1-BOC-4-PIPERIDYL)-ETHANAL ; TERT-BUTYL 4-(2-OXOETHYL)PIPERIDINE-1-CARBOXYLATE ; 4-(2-OXO-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER |
| MDL.： | MFCD03425258 |
| H bond acceptor： | 4 |
| H bond donor： | 0 |
| Smile： | CC(C)(C)OC(=O)N1CCC(CC1)CC=O |
| InChi： | InChI=1S/C12H21NO3/c1-12(2,3)16-11(15)13-7-4-10(5-8-13)6-9-14/h9-10H,4-8H2,1-3H3 |
| InChiKey： | InChIKey=PSRHRFNKESVOEL-UHFFFAOYSA-N |
Property |
|
| Melting Point： | 38-42 DEG C |
| Physical Property： | FLASHPOINT: >110 DEG C FLASHPOINT: >230 DEG F |
| Comments： | APPLICATION: BUILDING BLOCK EMPLOYED IN A SYNTHESIS OF (S)-QUINUCLIDINE-2-CARBOXYLIC ACID. SUBSTRATE USED IN AN ENANIOSELECTIVE ORGANO-CATALYTIC ALPHA-VINYLATION REACTION APPLICATION: REACTANT FOR SYNTHESIS OF: PIM-1 INHIBITORS. SELECTIVE GPR119 AGONISTS FOR TYPE II DIABETES. REACTANT FOR: ALPHA-ARYLATION OF ALDEHYDES. ENANTIOSELECTIVE ALPHA-BENZYLATION OF ALDEHYDES VIA PHOTOREDOX ORGANOCATALYSIS. ENANTIOSELECTIVE ALPHA-TRIFLOUROMETHYLATION OF ALDEHYDES UNSPSC: 12352100 WGK: 3 |
Safety information |
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N-BOC-4-PIPERIDINEACETALDEHYDE
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