trans-4-(Boc-aMino)-3-Methoxypiperidine

98%

Reagent Code: #151134
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CAS Number 1033748-33-2

science Other reagents with same CAS 1033748-33-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.3 g/mol
Formula C₁₁H₂₂N₂O₃
badge Registry Numbers
MDL Number MFCD22566136
thermostat Physical Properties
Boiling Point 332 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antidepressants and antipsychotics. Its trans-piperidine backbone with defined stereochemistry allows for selective interactions with biological targets. The Boc-protected amine enables stepwise synthesis in peptide-like structures or complex heterocycles, while the methoxy group can influence solubility and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and functional handles for further modification.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,730.00
inventory 1g
10-20 days ฿64,240.00

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trans-4-(Boc-aMino)-3-Methoxypiperidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antidepressants and antipsychotics. Its trans-piperidine backbone with defined stereochemistry allows for selective interactions with biological targets. The Boc-protected amine enables stepwise synthesis in peptide-like structures or complex heterocycles, while the methoxy group can influence solubility and binding affinity. Commonly employed in medicinal chemistry for struc

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antidepressants and antipsychotics. Its trans-piperidine backbone with defined stereochemistry allows for selective interactions with biological targets. The Boc-protected amine enables stepwise synthesis in peptide-like structures or complex heterocycles, while the methoxy group can influence solubility and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and functional handles for further modification.

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