| Identification | Back Directory | [Name]
1-N-BOC-3-BROMOPIPERIDINE | [CAS]
849928-26-3 | [Synonyms]
1-Boc-3-bromopiperidine
N-Boc-3-Bromopiperidine
1-N-BOC-3-BROMOPIPERIDINE
R-1-Boc-3-Bromopiperidine
S-1-Boc-3-Bromopiperidine
3-bromopiperidine-1-carboxylate
1-Piperidinecarboxylic acid, 3-broMo
tert-butyl 3-bromopiperidine-1-carboxylate
tert-butyl (S)-3-bromopiperidine-1-carboxylate
3-Bromo-1-piperidinecarboxylic acid tert-butyl ester
1-Piperidinecarboxylic acid, 3-bromo-, 1,1-dimethylethyl ester | [Molecular Formula]
C10H18BrNO2 | [MDL Number]
MFCD07779077 | [MOL File]
849928-26-3.mol | [Molecular Weight]
264.16 |
| Chemical Properties | Back Directory | [Boiling point ]
296.6±33.0 °C(Predicted) | [density ]
1.327 | [storage temp. ]
2-8°C | [pka]
-3.04±0.40(Predicted) | [InChI]
InChI=1S/C10H18BrNO2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h8H,4-7H2,1-3H3 | [InChIKey]
YCUDHDNCZHPAJK-UHFFFAOYSA-N | [SMILES]
N1(C(OC(C)(C)C)=O)CCCC(Br)C1 |
| Hazard Information | Back Directory | [Uses]
1-N-BOC-3-bromopiperidine is a valuable compound in organic synthesis, it is used as a protecting group for the piperidine nitrogen. | [Synthesis]
1-N-BOC-3-bromopiperidine can be synthesized from 3-bromopyrrolidine and sodium hydride in THF, and the BOC group can be removed using TFA. |
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