tert-Butyl 4-(2-aminopropan-2-yl)piperidine-1-carboxylate

97%

Reagent Code: #118528
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CAS Number 530116-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.36 g/mol
Formula C₁₃H₂₆N₂O₂
badge Registry Numbers
MDL Number MFCD22034255
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring and a tert-butyl group, makes it a valuable building block for creating compounds with potential therapeutic applications. It is often employed in the design and synthesis of drugs targeting neurological disorders, such as Alzheimer’s disease, due to its ability to modulate specific receptors in the brain. Additionally, it is used in the preparation of small molecule inhibitors and other pharmacologically active agents, contributing to advancements in medicinal chemistry. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,391.00
inventory 100mg
10-20 days ฿3,141.00
inventory 250mg
10-20 days ฿5,337.00
tert-Butyl 4-(2-aminopropan-2-yl)piperidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring and a tert-butyl group, makes it a valuable building block for creating compounds with potential therapeutic applications. It is often employed in the design and synthesis of drugs targeting neurological disorders, such as Alzheimer’s disease, due to its ability to modulate specific receptors in the brain. Additionally, it is used in the preparation of small molecule inhibitors and other pharmacologically active agents, contributing to advancements in medicinal chemistry. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.
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