tert-Butyl 4-(5-bromopyridin-2-yl)piperazine-1-carboxylate

98%

Reagent Code: #145765
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CAS Number 153747-97-8

science Other reagents with same CAS 153747-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.23 g/mol
Formula C₁₄H₂₀BrN₃O₂
thermostat Physical Properties
Melting Point 83-87°C
Boiling Point 433°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used as an intermediate in pharmaceutical synthesis, this compound plays a key role in the development of biologically active molecules, particularly kinase inhibitors and CNS-targeted drugs. Its piperazine core with a brominated pyridine moiety allows for selective cross-coupling reactions, enabling the introduction of diverse functional groups through palladium-catalyzed transformations. It is especially valuable in medicinal chemistry for constructing drug candidates targeting neurological disorders, inflammation, and certain cancers. The tert-butyl carbamate (Boc) protection ensures stability during multi-step syntheses and allows for controlled deprotection to reveal the amine for further derivatization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿546.00
inventory 25g
10-20 days ฿3,770.00
inventory 250mg
10-20 days ฿144.00

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tert-Butyl 4-(5-bromopyridin-2-yl)piperazine-1-carboxylate
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Widely used as an intermediate in pharmaceutical synthesis, this compound plays a key role in the development of biologically active molecules, particularly kinase inhibitors and CNS-targeted drugs. Its piperazine core with a brominated pyridine moiety allows for selective cross-coupling reactions, enabling the introduction of diverse functional groups through palladium-catalyzed transformations. It is especially valuable in medicinal chemistry for constructing drug candidates targeting neurological diso

Widely used as an intermediate in pharmaceutical synthesis, this compound plays a key role in the development of biologically active molecules, particularly kinase inhibitors and CNS-targeted drugs. Its piperazine core with a brominated pyridine moiety allows for selective cross-coupling reactions, enabling the introduction of diverse functional groups through palladium-catalyzed transformations. It is especially valuable in medicinal chemistry for constructing drug candidates targeting neurological disorders, inflammation, and certain cancers. The tert-butyl carbamate (Boc) protection ensures stability during multi-step syntheses and allows for controlled deprotection to reveal the amine for further derivatization.

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