S1146    

N-Boc-4-piperidone | 79099-07-3

Additional information

CAS ID

79099-07-3

IUPAC Name

tert-butyl 4-oxopiperidine-1-carboxylate

Molecular Formula

C10H17NO3

Molecular Weight

SMILES

CC(C)(C)OC(=O)N1CCC(=O)CC1

General Information

Additional information

CAS ID

79099-07-3

IUPAC Name

tert-butyl 4-oxopiperidine-1-carboxylate

Molecular Formula

C10H17NO3

Molecular Weight

SMILES

CC(C)(C)OC(=O)N1CCC(=O)CC1

Description

735900

Synonyms: 1-boc-4-piperidone, n-boc-4-piperidone, n-tert-butoxycarbonyl-4-piperidone, 1-boc-4-piperidinone, boc-4-piperidone, 1-tert-butoxycarbonyl-4-piperidone, n-boc-4-piperidinone, boc-piperidone, 1-t-boc-4-piperidone

Melting Point 75°C
Color Undesignated
Formula Weight 199.25
Physical Form Crystal-Powder at 20°C
Percent Purity ≥98.0% (GC)

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N-Boc-4-piperidone | 79099-07-3 FAQS

Boc Piperidone is used in chemical studies. It is an important step in making medicines, especially those with biological effects. Its piperidone structure makes it stable, which is helpful for complicated medical processes and the development of organic compounds.

The piperidone chemical structure includes a piperidine ring with a ketone group, making it very useful in organic chemistry reactions. Piperidone structure allows scientists to make specific changes, helping them create new compounds for medicine and industry.

The boc piperidone boiling point changes with air pressure, but it usually stays within a consistent range, making it easy to handle in labs. Accurate temperature data helps in making effective chemical mixtures and products.

The piperidone chemical formula is important for making medicines. Its flexible framework helps make changes that improve the effectiveness, stability, and precision of drugs in research.

To keep it safe, store boc piperidone in a dry place under controlled conditions. You need to wear the right safety gear because it can react. This ensures that you can handle it safely during experiments and when making things.