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CS-W001157 4
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tert-Butyl (3R,4S)-4-amino-3-hydroxypiperidine-1-carboxylate

  • CAS No. 1821799-48-7

  • Cat. No. CS-0052935
  • Purity≥96%
  • MDL No.MFCD27978551
  • HazMat Fee +

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    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

    There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

*For research and further manufacturing use only, not for direct human use.

tert-Butyl (3R,4S)-4-amino-3-hydroxypiperidine-1-carboxylate|CS-0052935

Structure of 1821799-48-7

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Description

tert-Butyl (3R,4S)-4-amino-3-hydroxypiperidine-1-carboxylate delivers a chiral piperidine scaffold with defined stereochemistry at C3 and C4. This bench-stable derivative features a hydroxyl group flanked by an amino function, enabling direct incorporation into complex molecular architectures. The tert-butyl carbamate protects the amine during synthetic manipulations while allowing straightforward deprotection under mild acidic conditions.

Application

tert-Butyl (3R,4S)-4-amino-3-hydroxypiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive piperidine derivatives. Its protected amine and hydroxyl groups enable orthogonal functionalization, while the (3R,4S) configuration supports predictable stereoselective transformations. The tert-butyl carbamate group provides bench stability and facilitates straightforward deprotection under mild acidic conditions, making it well-suited for iterative medicinal chemistry campaigns and API intermediate development.

General Information

  • CAS No. 1821799-48-7
  • Cat. No. CS-0052935
  • Purity ≥96%
  • MDL No. MFCD27978551
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₂₀N₂O₃
  • Molecular Weight 216.28
  • Synonym(s) (3R,4S)-1-Boc-4-amino-3-hydroxy-piperidine
  • SMILES CC(C)(C)OC(=O)N1CC[C@H](N)[C@H](O)C1

Computational Chemistry Data

  • TPSA   75.79
  • LogP   0.3154
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   0

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-P330-P362+P364-P405-P501

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