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Home/Compounds/Pharmaceutical Intermediate/(2S)-tert-Butyl 3-cyano-2-methyl-4-oxopiperidine-1-carboxylate
C12H18N2O3
238.28 g/mol
Pharmaceutical Intermediate

(2S)-tert-Butyl 3-cyano-2-methyl-4-oxopiperidine-1-carboxylate

CAS2212021-56-0
Category
Pharmaceutical Intermediate
Compound Class
Heterocycle
Primary Use
Pharmaceutical Intermediate

This compound is a protected piperidine derivative containing a nitrile and a ketone functional group. It is primarily used as an intermediate in pharmaceutical research and manufacturing.

pharmaceutical intermediateresearch compound for drug discovery

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

ReferenceSame Category

5H-Pyrazolo(4,3-c)pyridine-5-carboxylic acid, 3-(2,3-dihydro-2-oxo-1H-imidazol-1-yl)-2-(4-fluoro-3,5-dimethylphenyl)-2,4,6,7-tetrahydro-4-methyl-, 1,1-dimethylethyl ester, (4S)-

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ReferenceSame Category

Ethyl (S)-5-(2,2-dimethyltetrahydro-2H-pyran-4-yl)-1H-indole-2-carboxylate

CAS2212021-77-5

pharmaceutical intermediate

ReferenceSame Category

(S)-5-(2,2-Dimethyltetrahydro-2H-pyran-4-yl)-1H-indole-2-carboxylic acid

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pharmaceutical intermediate

ReferenceSame Category

(S)-1-(cyanomethyl)-5-(2,2-dimethyltetrahydro-2H-pyran-4-yl)-N-methyl-N-phenyl-1H-indole-2-carboxamide

CAS2212021-80-0

pharmaceutical intermediate

Referencesame scaffold

Tert-Butyl (2R)-2-methyl-4-oxopiperidine-1-carboxylate

CAS790667-43-5

pharmaceutical intermediate

Referencesame scaffold

Ethyl 4-oxo-1-piperidinecarboxylate

CAS29976-53-2

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Referencesame scaffold

{2,2,6,6-Tetrakis[(²H₃)methyl]-4-oxo(²H₄)piperidin-1-yl}oxidanyl

CAS36763-53-8

research compound

Referencesame scaffold

N-Methyl-3-carbomethoxy-4-piperidone hydrochloride

CAS13049-77-9

pharmaceutical intermediate

Identifiers
IUPAC Name

tert-butyl (2S)-3-cyano-2-methyl-4-oxopiperidine-1-carboxylate

InChIKey

HWSFSGRTZMJYGQ-IENPIDJESA-N

SMILES

C[C@H]1C(C(=O)CCN1C(=O)OC(C)(C)C)C#N

Synonyms (8)

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