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CS-W001157 4
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tert-Butyl (2R,4R)-4-amino-2-methylpiperidine-1-carboxylate

  • CAS No. 1691250-97-1

  • Cat. No. CS-0137893
  • Purity≥95%
  • MDL No.MFCD26954786
  • 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 (2R,4R)-4-amino-2-methylpiperidine-1-carboxylate|CS-0137893

Structure of 1691250-97-1

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Description

tert-Butyl (2R,4R)-4-amino-2-methylpiperidine-1-carboxylate is a stereochemically defined piperidine derivative featuring a bench-stable tert-butyl carbamate protecting group. This configuration enables efficient incorporation into complex molecular architectures, particularly in the synthesis of bioactive heterocycles and peptidomimetics. The amino functionality supports direct derivatization, while the methyl substituent enhances steric control during cyclization steps.

Application

tert-Butyl (2R,4R)-4-amino-2-methylpiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive piperidine derivatives. The protected amine and chiral methylpiperidine core enable direct incorporation into medicinal chemistry campaigns, facilitating efficient access to constrained scaffolds via standard coupling, alkylation, or reductive amination protocols. Bench-stable and compatible with diverse functional groups, it functions as a versatile intermediate in API development workflows requiring precise stereocontrol.

General Information

  • CAS No. 1691250-97-1
  • Cat. No. CS-0137893
  • Purity ≥95%
  • MDL No. MFCD26954786
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₂₂N₂O₂
  • Molecular Weight 214.30
  • Synonym(s) (2R,4R)-tert-butyl 4-amino-2-methylpiperidine-1-carboxylate
  • SMILES O=C(OC(C)(C)C)N1[C@@H](C[C@@H](CC1)N)C

Computational Chemistry Data

  • TPSA   55.56
  • LogP   1.7331
  • H_Acceptors   3
  • H_Donors   1
  • 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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