tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate

Name: tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate
Brand: ChemScene
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CAS No. 790667-99-1
Cat. No. CS-0048596
Purity≥97%
MDL No.None

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
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Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
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tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate|CS-0048596

Structure of 790667-99-1

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General Information

CAS No. 790667-99-1
Cat. No. CS-0048596
Purity ≥97%
MDL No. None
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₁H₂₁NO₃
Molecular Weight 215.29
Synonym(s) (2S,4S)-1-Boc-2-methyl-4-hydroxypiperidine
SMILES C[C@H]1C[C@@H](O)CCN1C(=O)OC(C)(C)C

Description

tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate is a chiral piperidine derivative featuring a bench-stable tert-butyl ester protecting group and a stereodefined hydroxyl moiety. This configuration enables direct incorporation into complex molecular scaffolds requiring precise stereocontrol. The molecule bears a reactive hydroxyl site for downstream functionalization while maintaining stability under standard handling conditions.

Application

tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate serves as a stereochemically defined chiral building block for the synthesis of bioactive molecules. The pendant hydroxyl group enables facile derivatization via esterification or ether formation, while the protected piperidine core exhibits excellent bench stability and compatibility with standard coupling reactions. Its functional group tolerance supports diverse transformations in medicinal chemistry workflows.

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-P280-P302+P352

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Computational Chemistry Data

TPSA 49.77
LogP 1.7667
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 0

Other Classifications

Building Blocks Functional Group Alcohol

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Aliphatic heterocycle compounds Piperidine compounds

Key Words

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tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate

CAS No. 790667-99-1

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