tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate

Name: tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate
Brand: ChemScene
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CAS No. 915226-43-6
Cat. No. CS-0079055
Purity≥97%
MDL No.None

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
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Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
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tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate|CS-0079055

Structure of 915226-43-6

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General Information

CAS No. 915226-43-6
Cat. No. CS-0079055
Purity ≥97%
MDL No. None
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₁H₂₀N₂O₃
Molecular Weight 228.29
Synonym(s) (R)-tert-Butyl 3-carbamoylpiperidine-1-carboxylate
SMILES O=C(N1C[C@H](C(N)=O)CCC1)OC(C)(C)C

Description

tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate is a stereochemically defined, bench-stable building block featuring a piperidine core with a carbamoyl group at the 3-position and a tert-butyl ester at the 1-position. This configuration supports efficient incorporation into bioactive molecule synthesis, particularly in medicinal chemistry campaigns requiring chiral piperidine scaffolds. The protected amine and polar carbamoyl moiety enable selective transformations under standard conditions.

Application

tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of piperidine-based pharmaceutical intermediates. Its carbamoyl group enables direct incorporation into bioactive scaffolds, while the tert-butoxycarbonyl (Boc) protection offers excellent bench stability and compatibility with standard peptide coupling and reduction protocols. The compound facilitates efficient access to chiral piperidine derivatives through orthogonal deprotection strategies and demonstrates broad functional group tolerance in multi-step syntheses.

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

TPSA 72.63
LogP 1.1188
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Amide

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Aliphatic heterocycle compounds Piperidine compounds

Key Words

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tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate

CAS No. 915226-43-6

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