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Home/Compounds/Research Reagent/1,1-Dimethylethyl 4-[[[(1R,2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl]amino]-1-piperidinecarboxylate
C17H28N4O5
368.4 g/mol
Research Reagent

1,1-Dimethylethyl 4-[[[(1R,2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl]amino]-1-piperidinecarboxylate

CAS1174020-64-4
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound

This compound is a research reagent featuring a tert-butyl carbamate-protected piperidine ring linked to a bicyclic diazabicyclo[3. 2.

laboratory research reagentsynthetic intermediate for pharmaceutical development

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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Referencesame scaffold

Relebactam

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Referencesame scaffold

Relebactam monohydrate

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pharmaceutical raw material

Customs Tariff Classification

The international HS code for 1,1-Dimethylethyl 4-[[[(1R,2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl]amino]-1-piperidinecarboxylate (CAS 1174020-64-4) is 2933.39.

HS code (international, 6-digit)

2933.39

EU CN code (8-digit)

2933 39 99

Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.

Identifiers
IUPAC Name

tert-butyl 4-[[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carbonyl]amino]piperidine-1-carboxylate

InChIKey

SXKJDJFTBGADNS-OLZOCXBDSA-N

SMILES

CC(C)(C)OC(=O)N1CCC(CC1)NC(=O)[C@@H]2CC[C@@H]3CN2C(=O)N3O

Synonyms (5)

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