tert-Butyl N-[(3S,4R)-4-hydroxypiperidin-3-yl]carbamate

95%

Reagent Code: #82801
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CAS Number 1549812-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.2779 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD30534444
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting central nervous system disorders, such as cognitive enhancers or neuroprotective agents. Its structure, featuring a piperidine ring and a carbamate group, makes it valuable for creating molecules with specific biological activity. Additionally, it is utilized in research and development for designing and optimizing drug candidates, especially those requiring precise stereochemistry for efficacy. Its applications extend to medicinal chemistry, where it contributes to the creation of novel therapeutics with improved pharmacological properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days €219.22
inventory 250mg
10-20 days €349.75
inventory 1g
10-20 days €1,069.00
tert-Butyl N-[(3S,4R)-4-hydroxypiperidin-3-yl]carbamate
This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting central nervous system disorders, such as cognitive enhancers or neuroprotective agents. Its structure, featuring a piperidine ring and a carbamate group, makes it valuable for creating molecules with specific biological activity. Additionally, it is utilized in research and development for designing and optimizing drug candidates, especially those requiring precise stereochemistry for efficacy. Its applications extend to medicinal chemistry, where it contributes to the creation of novel therapeutics with improved pharmacological properties.
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