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HomeProduct name listN-Boc-2-piperidone

N-Boc-2-piperidone

N-Boc-2-piperidone Structural

What is N-Boc-2-piperidone?

Chemical properties

Off-White Low Melting Solid

The Uses of N-Boc-2-piperidone

Intermediate in the preparation of various biological inhibitors.

What are the applications of Application

1-N-Boc-2-piperidone is a useful boc protected biochemical for proteomics research

Definition

ChEBI:N-Boc-2-piperidone-protected by t-Boc. It is also known as 1-N-Boc-2-piperidone,1-N-Boc-2-piperidone, or 1-(tert-Butoxycarbonyl)-2-piperidone. 

Preparation

4-Benzensulfonylmethyl-4-hydroxy-piperidine TFA (B-1) Diisopropylethylamine (28.3 mL, 162.75 mmol) and di-t-butyl dicarbonate (28.4 g, 130.02 mmol) were added in sequence to a mixture of piperidone hydrate hydrochloride (12) (10.0 g, 65.1 mmol) in methanol (50 mL).  The mixture was stirred at room temperature for 20 hours. After that, removed the solvent  and the remaining was separated with ether and 1 M KHSO4 solution.  The organic layer was washed with brine and saturated NaHCO3.  Finally, N-Boc-2-piperidone was obtained after purification.
N-Boc-2-piperidone

Properties of N-Boc-2-piperidone

Melting point: 29-36 °C
Boiling point: 110°C/0.1mmHg(lit.)
Density  1.099±0.06 g/cm3(Predicted)
Flash point: >110 °C
storage temp.  Keep in dark place,Sealed in dry,Room Temperature
solubility  Chloroform, Methanol
form  Solid
pka -2.29±0.20(Predicted)
color  Off-White Low Melting
BRN  4674955
InChI InChI=1S/C10H17NO3/c1-10(2,3)14-9(13)11-7-5-4-6-8(11)12/h4-7H2,1-3H3
CAS DataBase Reference 85908-96-9(CAS DataBase Reference)

Safety information for N-Boc-2-piperidone

Signal word Warning
Pictogram(s)
ghs
Environment
GHS09
GHS Hazard Statements H410:Hazardous to the aquatic environment, long-term hazard
Precautionary Statement Codes P273:Avoid release to the environment.
P391:Collect spillage. Hazardous to the aquatic environment
P501:Dispose of contents/container to..…

Computed Descriptors for N-Boc-2-piperidone

InChIKey ULMHMJAEGZPQRY-UHFFFAOYSA-N
SMILES N1(C(OC(C)(C)C)=O)CCCCC1=O

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